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CN100412082C - Cyclo-glycosyl amino acid, its preparation method and usage in preventing and curing heavy metal poisoning - Google Patents

Cyclo-glycosyl amino acid, its preparation method and usage in preventing and curing heavy metal poisoning Download PDF

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CN100412082C
CN100412082C CNB2003101004266A CN200310100426A CN100412082C CN 100412082 C CN100412082 C CN 100412082C CN B2003101004266 A CNB2003101004266 A CN B2003101004266A CN 200310100426 A CN200310100426 A CN 200310100426A CN 100412082 C CN100412082 C CN 100412082C
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sugar ring
ortho
ethanoyl
amino acid
nitrophenyl
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CN1607206A (en
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彭师奇
王超
赵明
霍彩霞
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Pharmaceutical Technology Development Branch Beijing Beiyi Investment And Manag
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Abstract

The present invention relates to novel heavy metal excretion prompting agent of pyran glucosyl amino acid and pyran arabinose glycosyl amino acid, a preparing method thereof and an application of the pyran glucosyl amino acid and the pyran arabinose glycosyl amino acid and compounds containing the pyran glucosyl amino acid and the pyran arabinose glycosyl amino acid in curing and preventing heavy metal poisoning.

Description

Cyclohexanol base amino acid and preparation method thereof and the purposes of preventing and treating heavy metal poisoning
Technical field
The present invention relates to novel glucopyranosyl amino acid of a class and arabinofuranosyl amino-acid compound, their synthetic method and they treat and/or prevent purposes in the medicine of heavy metal poisoning in preparation.
Background technology
Almost always and everywhere bear the injury of various approach heavy metal contaminations.The heavy metal that wherein with lead is representative has been a public cognitive to the harm of human body.Plumbous pollution channel to environment almost spreads all over whole human living space, comprises atmosphere Lead contamination, drinking-water Lead contamination, soil Lead contamination and household utensils Lead contamination.The cigarette that with lead is food, the inhaled air of utensil by using of the heavy metal of representative, absorption, the water of drinking, suction enters human body.Heavy metal distributes and storage by absorbing after entering human body to change, is accumulated among the important organ.The lead that for example enters human body has at least 90% to be deposited in the bone.Lead enter after the cell can with organoid and protein bound, remove and change in the human body the proteic structure of normal function and activity all right intravital a series of peroxidatic reaction of lipid of catalysis.So except plumbous itself directly tissue and the organ toxicity, the serious consequence that tumour, cardiovascular disorder and the geriatric disease that is caused by the lipid peroxidation of metal catalytic causes also is in the state of extensively not paid attention to.Since plumbous can length up to standard 1460 days in the intravital transformation period of people, so though the general trend that lead is accumulated in the human body is to increase at the age and increase.
Though serious acute lead poisoning case often appears among the resident of manufacturing district of plumbous steam and lead fume dirt discharging, the air Lead contamination that is caused by automobile exhaust gas reaches the water source Lead contamination that is caused by trade effluent and can cause non-manufacturing district big area crowd's chronic lead poisoning.Though children are because to eat the lead poisoning case that takes place from the leaded coating agent which has to be dissolved in alcohol before use in toy, furniture, wall and the soil by mistake actually rare, but can cause the extensive chronic lead poisoning of seeing from the lead of porcelain, food and drink, apparatus more.
The Signs that causes by direct lead poisoning have poor appetite, insomnia, headache, dizziness, muscle and joint pain, stomachache, constipation, belch and mouthful in metal peculiar smell etc.The neural system toxicity that is caused by direct lead poisoning has corticocerebral excitement and process of inhibition disorder, cortex-internal organ insufficiency of accommodation, neurasthenia disease group occurs, and toxic polyneuritis and toxic encephalopthy.
At present the saturnine medicine of clinical treatment can be divided into two types of ammonia carboxylic type compound and sulfhydryl compounds by structure.Ammonia carboxylic type compound has calcium disodium edetate (Na 2Ca-EDTA) and calcium trisodium pentetate (CaNa 3-DTPA).Sulfhydryl compound has Trolovol and sodium dimercaptosuccinate.These medicines are except that can not be oral and be difficult to stride across and also have shortcomings such as poor selectivity and toxic side effect are big the cytolemma.Searching can be oral, selectivity is high, toxic side effect is little and stride the good lead poisoning toxinicide of film properties, and clear and definite application prospect is arranged.
Summary of the invention
The purpose of this invention is to provide structure is the amino acid whose oral heavy metal eccritic of glucopyranosyl amino acid and arabinofuranosyl.
Glucopyranosyl amino acid of the present invention has following general formula (I) and (II):
Figure C20031010042600062
Arabinofuranosyl amino acid of the present invention has following structural formula (III) and (IV):
Figure C20031010042600063
Wherein above various in, R is a hydrogen, replaces or non-substituted alkyl, especially non-replacement or replace the C1-C10 alkyl replaces or non-substituted aralkyl, replaces or non-substituted heterocycle group alkyl sulfhydryl group, sulfide group, amide group, acidic group, amido etc.
Preferably, R=H ,-CH3 ,-CH 2OH ,-CH (OH) CH 3,-CH 2SH ,-CH 2CH 2SCH 3,-CH (CH 3) 2,-CH 2CH (CH 3) 2,-CH 2COOH, indoles methylene radical ,-CH 2CH (CH 3) 2,-CH 2(CH 3) CH 2CH 3,-CH 2(C 6H 5), para hydroxybenzene methylene radical ,-CH 2C (O) NH 2,-CH 2CH 2C (O) NH 2,-CH 2CH 2COOH ,-CH 2CH 2CH 2CH 2NH 2,-CH 2CH 2CH 2NHC (=NH) NH 2Deng.
The compound name that the compound name that the compound name that the compound name of general formula (I) is called N-α-Glucopyranose-2-base-L-amino acid, general formula (II) is called N-β-Glucopyranose-2-base-L-amino acid, general formula (III) is called N-α-Fu Nan pectinose-1-base-L-amino acid and general formula (IV) is called N-β-furans pectinose-1-base-L-amino acid.L-amino acid wherein comprises glycine, L-L-Ala, L-Serine, L-Threonine, L-halfcystine, L-methionine(Met), L-Xie Ansuan, L-leucine, L-aspartic acid, L-tryptophane, the L-leucine, the L-leucine, the L-Isoleucine, L-phenylalanine, L-L-glutamic acid, altheine, L-glutaminate, L-arginine etc., or the amino acid whose derivative of these L-.
Another object of the present invention provides the preparation method of the compound of above general formula (I)-(IV).
General formula of the present invention (I) and preparation method (II) comprise:
A, allow the reaction of the L-amino acid tert-butyl ester and ortho-nitrophenyl SULPHURYL CHLORIDE, make N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
B, allowing the reaction of D-glucose and glacial acetic acid, make 2,3,4,6-O-is tetra-acetylated-the D-Glucopyranose;
C, 2,3,4,6-four-O-ethanoyl-D-Glucopyranose and N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester reaction makes epimerization blended N-2,3,4, the 6-four-O-ethanoyl-D-Glucopyranose-1-base-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
D, obtain N-2 through separation, 3,4,6-four-O-ethanoyl-α-D-Glucopyranose-1-base-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid the tert-butyl ester and N-2,3,4, the 6-four-O-ethanoyl-β-D-Glucopyranose-1-base-N-ortho-nitrophenyl alkylsulfonyl-1-amino acid tert-butyl ester;
E, the α that obtains and beta isomer respectively deprotection (for example with the tertiary butyl in the acid of trifluoroacetic acid deaminizating, with the ethanoyl on the sodium methylate desugar ring, with the ortho-nitrophenyl alkylsulfonyl on two isopropylamine (DIPEA) of N-ethyl and the sour N of thiophenol deaminizating; when amino-acid residue takes off tertiary butyl protection on the sulfydryl with ortho-nitrophenyl base sulphinyl chlorine and sodium borohydride during for halfcystine), make N-(α-D-1-deoxidation pyranofructose-1-yl)-L-amino acid and N-(β-D-1-deoxidation pyranofructose-1-yl)-L-amino acid.
In the reaction of the L-amino acid tert-butyl ester and ortho-nitrophenyl SULPHURYL CHLORIDE, the alkali that is used for absorbing hydrogen chloride comprises organic bases that triethylamine, Dimethylamino pyridine, pyridine etc. are general and solid NaOH, KOH, LiOH, Ca (OH) 2, NaCO 3And NaHCO 3The mineral alkali of one class.Solvent comprises anhydrous CH 2Cl 2, CHCl 3, ethyl acetate, toluene and tetrahydrofuran (THF) one class inert organic solvents.
When preparation 1,2,3,4,6-five-O-ethanoyl-D-Glucopyranose, D-glucose, anhydrous sodium acetate and diacetyl oxide reflux at least 2 hours are utilized self heat release reflux at least 2 hours then then.Therefore the reaction times is 4-8 hour.The solvent that is used for the crude product recrystallization is the alcohols of anhydrous methanol, dehydrated alcohol and anhydrous isopropyl alcohol one class.
When preparation 2,3,4,6-four-O-ethanoyl-D-Glucopyranose, solvent is anhydrous tetrahydro furan, CH 2Cl 2, CHCl 3The organic solvent of one class.
2,3,4, when 6-four-O-ethanoyl-D-Glucopyranose and N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester reacted, solvent was new anhydrous tetrahydro furan, the CH that steams 2Cl 2, CH 3Cl 3And the inert organic solvents of glycol dimethyl ether one class.Phosphine with triphenylphosphine one class is a catalyzer, with N 2And Ar 2The protection of inert gas of one class is-50 ℃ to-80 ℃ reactions down.Reaction times is 1-8 hour.Use ordinary silicon plastic column chromatography or flash silica gel column chromatography when separating α and two kinds of epimerization products of β, the mixed solvent that adopts hexanaphthene and ethyl acetate, sherwood oil and ethyl acetate, sherwood oil and ether or hexanaphthene and ether is by the proper proportion wash-out.Lock out operation is at normal pressure or add to depress and carry out.
N-(2; 3; 4; 6-four-O-ethanoyl-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-when the L-amino acid tert-butyl ester takes off the tertiary butyl with trifluoroacetic acid; trifluoroacetic acid is again a reaction solvent simultaneously; consumption is doubly measured calculating by the 5-8 of raw material, and temperature of reaction is 10-20 ℃, and the reaction times is 1-6 hour.Thick product is with ordinary silicon plastic column chromatography or flash silica gel column chromatography purification, adopt the hexanaphthene that contains an amount of glacial acetic acid and ethyl acetate, sherwood oil and ethyl acetate, sherwood oil and ether or hexanaphthene in the mixed solvent of ether in an amount of ratio proportioning wash-out.Column chromatography normal pressure or in depress and carry out.
N-(2; 3; 4; 6-four-O-ethanoyl-D-Glucopyranose-1-yl)-when N-(ortho-nitrophenyl alkylsulfonyl)-L-amino acid is protected with the sodium methylate deacetylation; solvent anhydrous methanol solvent needs new the steaming, and temperature of reaction is-4 ℃-4 ℃, and the consumption of sodium methylate doubly calculates by the 1.2-1.9 of raw material; the PH of reactant is 9.5-11.5, and the reaction times is 12-36 hour.When reaction finished, reaction mixture was transferred PH2.5-5.5 with acidic cation-exchange resin.
N-(D-Glucopyranose-1-yl)-when N-(ortho-nitrophenyl alkylsulfonyl)-L-amino acid takes off ortho-nitrophenyl alkylsulfonyl protecting group with diisopropyl ethyl amine and thiophenol, reaction solvent are anhydrous dimethyl formamide or dioxane, Ar 2Or N 2Protection, temperature of reaction are that 10 ℃-18 ℃, reaction times are 1.5-8 hour.
General formula of the present invention (III) and preparation method (IV) comprise:
A, allow the reaction of the L-amino acid tert-butyl ester and ortho-nitrophenyl SULPHURYL CHLORIDE, make N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
B, allow the reaction of D-pectinose and glacial acetic acid, make 2,3,5-three-O-ethanoyl-D-furans pectinose;
C, 2,3,5-three-O-ethanoyl-D-furans pectinose and N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester reaction makes epimeric blended N-(2,3,5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
D, obtain N-(2 through chromatographic separation, 3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester and N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
E, the α that obtains and beta isomer deprotection (for example respectively with the tertiary butyl in the acid of trifluoroacetic acid deaminizating, with the ethanoyl on the sodium methylate desugar ring, with the ortho-nitrophenyl alkylsulfonyl on two sec.-propyl ethylamines (DIPEA) of N-and the sour N of thiophenol deaminizating; when amino-acid residue is halfcystine; take off tertiary butyl protecting group on the sulfydryl with ortho-nitrophenyl base sulphinyl chlorine and sodium borohydride), make N-(α-D-1-deoxidation ketofuranose-1-yl)-L-amino acid and N-(β-D-1-deoxidation ketofuranose-1-yl)-L-amino acid.
In the reaction of the L-amino acid tert-butyl ester and ortho-nitrophenyl SULPHURYL CHLORIDE, the alkali that is used for absorbing hydrogen chloride comprises organic bases that triethylamine, Dimethylamino pyridine and pyridine are general and solid NaOH, KOH, LiOH, Ca (OH) 2, Na 2CO 3And NaHCO 3The mineral alkali of one class.Solvent comprises anhydrous CH 2Cl 2, CHCl 3, ethyl acetate, toluene and tetrahydrofuran (THF) one class inert organic solvents.
When preparation 1,2,3,5-four-O-ethanoyl-D-furans pectinose, D-pectinose, diacetyl oxide and pyridine reacted 30 hours in room temperature then at least 90 ℃-110 ℃ heating at least earlier 6 hours.
When preparation 2,3,5-three-O-ethanoyl-D-furans pectinose, solvent is anhydrous tetrahydro furan, CH 2CL 2And CHCL 3The organic solvent of one class.
2,3, when 5-three-O-ethanoyl-D-furans pectinose and N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester reacted, solvent was new anhydrous tetrahydro furan, the CH that steams 2Cl 2, CHCl 3, and the inert organic solvents of glycol dimethyl ether one class.Phosphorus with triphenyl phosphorus one class is catalyzer, with N 2And Ar 2The protection of inert gas of one class; reacted at least 2 hours with waiting in the presence of the mole diisopropyl azodiformate (DIAD) at-50 ℃ to-80 ℃; at least reacted under the room temperature 20 hours then. when separating α and two kinds of epimerization products of β; use ordinary silicon plastic column chromatography or flash silica gel column chromatography, adopt hexanaphthene to mix by the suitable proportion proportioning with the mixed solvent of ether with ether or hexanaphthene with ethyl acetate, sherwood oil with ethyl acetate, sherwood oil.Lock out operation normal pressure or in depress and carry out.
N-(2; 3; 5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-when the L-amino acid tert-butyl ester takes off the tertiary butyl with trifluoroacetic acid; trifluoroacetic acid is again a reaction solvent simultaneously; consumption is pressed the 5-8 amount of raw material and is calculated; temperature of reaction is 10 ℃-20 ℃, and the reaction times is 1-6 hour.Thick product is with ordinary silicon plastic column chromatography or flash silica gel column chromatography purification, and the mixed solvent that adopts the hexanaphthene that contains glacial acetic acid and ethyl acetate, sherwood oil and ethyl acetate, sherwood oil and ether or hexanaphthene and ether is by proper proportion proportioning wash-out.Column chromatography operate in normal pressure or in depress and carry out.
N-(2; 3; 5-three-O-ethanoyl-D-furans pectinose-1-yl)-when N-(ortho-nitrophenyl alkylsulfonyl)-L-amino acid is protected with the sodium methylate deacetylation; the solvent anhydrous methanol needs new the steaming; temperature of reaction is-4 ℃-4 ℃; the consumption of sodium methylate doubly calculates by the 1.2-1.9 of raw material, and the pH of reactant is 9.5-11.5, and the reaction times is 12-36 hour.When reaction finished, reaction mixture was transferred pH2.5-5.5 with acidic cation-exchange resin.
N-(D-furans pectinose-1-yl)-when N-(ortho-nitrophenyl alkylsulfonyl)-L-amino acid takes off ortho-nitrophenyl alkylsulfonyl protecting group with diisopropyl ethyl amine and thiophenol, reaction solvent are dimethyl formamide or dioxane, Ar 2Or N 2Protection, temperature of reaction are that 10 ℃-18 ℃, reaction times are 8-15 hour.
Another purpose of the present invention provides the purposes of above-claimed cpd in preparing the medicine that treats and/or prevents heavy metal poisoning.
A further object of the present invention provides the pharmaceutical composition of the above-claimed cpd that contains significant quantity.Composition of the present invention can also comprise carrier and optional additive such as flavouring agent, sweeting agent etc.The content of compound in pharmaceutical composition of its formula of (I)-(IV) for example can be 1-95%.
Pharmaceutical composition of the present invention can be made oral dosage form or injection or transfusion formulation.Oral dosage form preferably.
The compound of general formula of the present invention (I)-(IV) can one or more use alone, or uses with the form that contains one or more compound compositions.
The dosage of the compound of general formula of the present invention (I)-(IV) decides according to the factors such as weight of patient age, body weight, the course of disease, disease.For example, as a reference, under the situation of oral dosage form, the consumption of compound of the present invention can be 0.1-10mg/kg/d, and under the situation of injection type, compound amount of the present invention can be 0.05-5mg/kg/d.
In following examples, the present invention has synthesized N-α-Glucopyranose-2-base-L-amino acid (I a according to route 1 and route 2, d, e), N-β-Glucopyranose-2-base-L-amino acid (II a-e), N-α-Fu Nan pectinose-1-base-L-amino acid (IIIa-f) and N-β-furans pectinose-1-base-L-amino acid (IV b-e):
Figure C20031010042600101
Figure C20031010042600102
The compound of mutual-through type of the present invention (I-IV) has carried out experimentation on animals, and the result shows that the lead content of accumulating in multiple internal organs of mouse and bone can be obviously lowered in compound oral administration of the present invention administration.Compound of the present invention is during treating, and the lead content in the blood of animal, ight soil and the urine obviously increases.Thereby compound of the present invention has clear and definite plumbous decorporation ability.
With the blank group relatively, compound of the present invention does not have obvious influence to the content of the iron in the mouse kidney, copper, zinc, manganese and calcium, thereby compound of the present invention is optionally plumbous in the drive row kidney.
The Kunming mouse oral administration once gives compound dosage of the present invention up to the 3.2g/Kg body weight, none death of animal.Thereby compound of the present invention is a low toxicity compounds.
In the experiment of short cadmium drive row, compound exhibits of the present invention same obvious treatment effect.
The constructional feature of compound of the present invention is to contain α-D-1-deoxidation pyranofructose base, β-D-1-deoxidation pyranofructose base, α-D-1-deoxidation furanone glycosyl, β-D-1-deoxidation furanone glycosyl in the molecule, and various a-amino acid residue.Compare with existing heavy metal decorporation medicine, they can be oral, and short heavy metal discharge capacity is strong, and selectivity is high and toxicity is low.
New compound of the present invention can be used for preparing oral decorporation heavy metal medicine, healthcare products and protective foods.New compound of the present invention further can be used for preparing medicine, healthcare products and the protective foods of oral lead discharging, and the medicine, healthcare products and the protective foods that are used to prepare decorporation cadmium, mercury, lead, antimony and arsenic.
Route 1:N-(1-deoxidation-D-pyranofructose-1-yl)-amino acid whose synthetic route of L-
Figure C20031010042600111
Fig. 1, N-(1-deoxidation-D-pyranofructose-1-yl)-amino acid whose synthetic route of L-
Route 2:N-(D-furans pectinose-1-the yl)-amino acid whose synthetic route of L-
Figure C20031010042600121
Embodiment
The invention will be further described below by embodiment.Should be pointed out that these embodiment only are illustrations of the present invention, should not be construed as limitation of the present invention.
The preparation of embodiment 1L-aspartic acid di tert butyl carbonate
3.99g (30mmol) mixture of L-aspartic acid, 412ml (66mmol) perchloric acid and 168ml tert.-butyl acetate, stirring at room are placed in refrigerator after 48 hours and are spent the night.Reaction mixture washes (4 * 100ml) with dilute hydrochloric acid (0.5mol/l).Isolating water layer solid NaHCO 3Be neutralized to PH7-8, and the usefulness ethyl acetate extraction (8 * 50ml), the saturated NaHCO of the ethyl acetate layer of merging 3The aqueous solution wash (2 * 200ml), anhydrous Na 2SO 4Drying is filtered, and filtrate decompression concentrates, and the hydrochloride 6.4g (76%) that obtains title compound is a light yellow solid.Rf (petrol ether/ethyl acetate, 2: 1) is 0.26.Product is not purified, is directly used in next step reaction.
The preparation of the embodiment 2L-S-tertiary butyl halfcystine tert-butyl ester
Press the operation of embodiment 1, replace the L-aspartic acid with 4.80g (30mmol) L-S-tertiary butyl halfcystine, obtaining title compound 5.7g (71%) is light yellow solid.Rf (petrol ether/ethyl acetate, 2: 1) is 0.3.Product is not purified, is directly used in the next step.
The preparation of embodiment 3L-L-glutamic acid di tert butyl carbonate
Press the operation of embodiment 1, replace the L-aspartic acid, obtain title compound 6.2g (80%), be light yellow solid with 4.41g (30mmol) L-L-glutamic acid.Rf (petrol ether/ethyl acetate, 2: 1) is 0.15.Product is not purified, is directly used in next step reaction.
The preparation of the embodiment 4L-O-tert-butyl serine tert-butyl ester
Press the operation of embodiment 1, replace the L-aspartic acid, obtain title compound 4.95g (76%), be light yellow solid with 4.83g (30mmol) L-Serine.Rf (petrol ether/ethyl acetate, 2: 1) is 0.35.Product is not purified, is directly used in next step reaction.
The preparation of the embodiment 5L-phenylalanine tert-butyl ester
Press the operation of embodiment 1, replace the L-aspartic acid, obtain title compound 5.28g (80%), be light yellow solid with 4.95g (30mmol) L-phenylalanine.Rf (petrol ether/ethyl acetate, 2: 1) is 0.4.Product is not purified, is directly used in next step reaction.
The preparation of embodiment 6L-O-tertiary butyl threonine tert-butyl ester
According to the operation of embodiment 1, replace the L-aspartic acid with 5.25g (30mmol) L-Threonine, obtain title compound 5.20g (75%), be light yellow solid.Rf (petrol ether/ethyl acetate, 2: 1) is 0.31.Product is not purified, is directly used in next step reaction.
The preparation of embodiment 7N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate
2.80g (10mmol) solution of hydrochloric acid L-aspartic acid di tert butyl carbonate, 2ml triethylamine, 0.33g (2mmol) 4-Dimethylamino pyridine and 100ml anhydrous methylene chloride is in stirring at room after 15 minutes, ice bath cooling, gradation inward add 2.22g (10mmol) ortho-nitrophenyl SULPHURYL CHLORIDE.The reaction mixture stirring at room is evaporated to dried after 3 hours, residue 100ml acetic acid ethyl dissolution.The solution that obtains successively with saturated NaCl solution wash (2 * 50ml), saturated KHSO 4Solution wash (3 * 50ml) and saturated NaCl solution wash (2 * 50ml).Isolating ethyl acetate layer anhydrous Na 2SO 4Dry, filter, be evaporated to dried, obtain title compound 3.87g (90%), be buff powder.Rf (petrol ether/ethyl acetate, 2: 1) is 0.3, mp 107-108 ℃.
The preparation of embodiment 8N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester
According to the operation of example 7, replace hydrochloric acid L-aspartic acid di tert butyl carbonate to obtain title compound 3.97 (95%) with the hydrochloric acid L-S-tertiary butyl-L-halfcystine tert-butyl ester 2.69g (10mmol), be pale brown look solid.Rf (petrol ether/ethyl acetate, 2: 1) is 0.25, mp 97-100 ℃. 1HNMR (500MHz, CDCI 3), δ 8.12-8.14 (d, J=10Hz, 1H, Phe H 3), 7.56-7.60 (m, 1H, phe H 6), 7.28-7.32 (m, 2H, pheH 4And H 5), 6.32 (d, J=5Hz, 1H, NH), 4.32 (m, 1H, cysC α H), 3.56 (dd, J=5.5, J=13.5Hz, 1H, CH 2), 3.44 (dd, J=5.5, J=13.5Hz, 1H, CH 2), 1.3 (S, 18H, 3 * CH 3).
The preparation of embodiment 9N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate
According to the operation of embodiment 7, replace L-aspartic acid di tert butyl carbonate with hydrochloric acid l-glutaminic acid di tert butyl carbonate 2.96g (10mmol), obtain 4.0g (90%) title compound, mp 101-103 ℃, Rf (petrol ether/ethyl acetate, 2: 1) is 0.28.
The preparation of embodiment 10N-(ortho-nitrophenyl alkylsulfonyl)-L-O-tert-butyl serine tert-butyl ester
According to the operation of embodiment 7, replace L-aspartic acid di tert butyl carbonate with hydrochloric acid L-O-tert-butyl serine tert-butyl ester 2.53g (10mmol), obtain 3.78g (94%) title compound, mp 103-104 ℃, Rf (petrol ether/ethyl acetate, 2: 1) is 0.28. 1HNMR(300MHz，CDCI 3)8.08-8.10(d，J＝10Hz，1H，Phe?H 3)，7.93-7.95(m，1H，phe?H 6)，7.74-7.77(m，2H，pheH 4，phe?H 5)，6.37(d，J＝5Hz，1H，NH)，4.23-4.26(m，1H，serCαH)，3.79(dd，J＝3Hz，J＝8.5Hz，1H，CH 2)，，3.61(dd，J＝3Hz，J＝8.5Hz，1H，CH 2)，1.28(S，9H，3×CH 3)，1.09(S，9H，3×CH 3)。
The preparation of embodiment 11N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester
According to the operation of embodiment 7, replace L-aspartic acid di tert butyl carbonate with hydrochloric acid L-phenylalanine tert-butyl ester 2.58g (10mmol), obtain 3.74g (92%) title compound, mp 92-93 ℃, Rf (petrol ether/ethyl acetate, 2: 1) is 0.40.
The preparation of embodiment 12N-(ortho-nitrophenyl alkylsulfonyl)-L-O-tertiary butyl threonine tert-butyl ester
According to the operation of embodiment 7, replace L-aspartic acid di tert butyl carbonate with hydrochloric acid L-O-tertiary butyl threonine tert-butyl ester 2.68g (10mmol), obtain 3.91g (94%) title compound, mp 87-90 ℃, Rf (petrol ether/ethyl acetate, 2: 1) is 0.40.
Embodiment 131,2,3,4, the preparation of 6-five-O-ethanoyl-D-Glucopyranose
Gradation adds 40g (22.2mmol) D-glucose in the suspension of the 12g anhydrous sodium acetate of reflux and 600ml diacetyl oxide, lasts 2 hours.Exothermic heat of reaction refluxes and aggravates therebetween.Continued reflux afterwards 2 hours, the color and luster of reaction mixture deepens gradually, and the final reaction mixture is brown.Stopping after the heating is to make reaction mixture be cooled to about 40 ℃ naturally.In the reaction mixture impouring frozen water, stir simultaneously.The oily matter of waiting to sink in the frozen water solidifies filter collection throw out afterwards, is the khaki color powder.(2 * 200ml), the organic layer of merging is used earlier saturated NaHCO to filtrate with ethyl acetate extraction 3The aqueous solution wash (2 * 100ml), be washed till neutrality with distilled water again, use MgSO then 4Drying is filtered, and filtrate decompression is concentrated into dried.Residue that obtains and the khaki color powder ethyl alcohol recrystallization that direct filter collects obtain 35g (40.4%) title compound, are white solid.Thin-layer chromatography (petrol ether/ethyl acetate 2: 1) launches twice, and the Rf of αYi Gouti is 0.68, and the Rf of beta isomer is 0.63, α: β=1: 8.
Embodiment 14 2, and 3,4, the preparation of 6-four-O-ethanoyl-D-Glucopyranose
0.69ml (10mmol) solution of quadrol and 10ml anhydrous tetrahydro furan at room temperature uses 0.57ml (10mmol) glacial acetic acid to handle stirring at room 30 minutes.In this solution, add 3.9g (10mmol) 1,2,3,4,6-five-O-ethanoyl-D-Glucopyranose, stirring at room 12 hours, thin-layer chromatography (petrol ether/ethyl acetate, 2: 1) shows that raw material point disappears.Reaction mixture is evaporated to dried, and residue is with the dilution of 200ml ethyl acetate, the solution that obtains successively with saturated Nacl solution wash, saturated NaHCO 3The aqueous solution is washed, 5% salt pickling, saturated NaCl solution are washed, anhydrous MgSO 4Dry.Filter, filtrate decompression is concentrated into dried, obtains 3.3g (94%) title compound, is the buff syrup thing.Rf (petrol ether/ethyl acetate, 2: 1) is 0.23.
Embodiment 15N-(2; 3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate and N-(2; 3; 4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-preparation of N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate
1.74g (5mmol) 2,3,4,5-four-O-ethanoyl-D-Glucopyranose, 1.30g (5mmol) triphenylphosphine, 2.34g (5mmol) hydrochloric acid N-(ortho-nitrophenyl alkylsulfonyl)-L-acid tert-butyl and 30ml newly steam the solution of anhydrous tetrahydro furan at Ar 2Protection was stirred 15 minutes with-80 ℃ down.In reaction mixture, add 0.97ml (5mmol) diisopropyl azodiformate rapidly.Reaction mixture was warming up to room temperature at least 2 hours, continue then to stir 12 hours, and TLC (petrol ether/ethyl acetate, 2: 1) shows that raw material point disappears.Reaction mixture is evaporated to dried, and residue is at 0.5Kg/cm 2Column chromatography for separation under the pressure; developping agent is a cyclohexane/ethyl acetate; 2: 1; obtain N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate 809mg (21.3%) and N-(2; 3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate 2839mg (74.7%).
N-(2,3,4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate: Rf (cyclohexane/ethyl acetate, 2: 1) is 0.25, mp 68-70 ℃, [α] D 20=+6.0 (C=1, CHCI 3). 1H NMR (300MHz, CDCI 3) δ 8.15-8.18 (m, 1H, pheH 3), 7.71-7.75 (m, 2H, pheH 4, H 6), 7.57-7.6 (m, pheH 5) 5.68 (d, J=2.4Hz, 1H, sugar ring H 1), 5.19 (dd, J=2.4Hz, J=10.1Hz, 1H, sugar ring H 2), 5.10 (t, J=3Hz, 1H, sugar ring H 3) 4.92-4.96 (m, 2H, sugar ring H 4And H 5), 4.32-4.36 (m, 1H, Asp C α H), 4.26 (dd; J=4.5Hz, J=12Hz, sugar ring H6a), 4.16 (dd; J=5.4Hz, J=12Hz, sugar ring H6b), 3.28 (dd; J=10.2Hz, J=16.2Hz, 1H, AspC β H); 2.68 (dd, J=3Hz, J=16.2Hz, 1H; AspC β H), 2.02-2.16 (m, 12H, 4 * CH of sugar ring ethanoyl 3), 1.48 (S, 9H, 3 * CH 3), 1.45 (S, 9H, 3 * CH 3). 13CNMR (300MHz, CDCI 3) δ 170.5,169.9,169.2,168.9,168.8,168.5,143.6,134.2,132.4,131.9,131.0,123.8,83.0,81,73.5,78.2,70.3,69.8,61.4,56.2,67.0,39,28.1,27.7,21.04,21.07,21.069.
N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate: Rf (cyclohexane/ethyl acetate, 2: 1) is 0.27, mp67-69 ℃, [α] D 20=+73 (C=1.3, CHCL 3). 1HNMR (300MHz, CDCI 3) δ 8.25-8.27 (d, J=7.8Hz, pheH 3), 7.57-7.72 (m, 3H, pheH 4, pheH 5And pheH 6), 5.55 (m, 1H, sugar ring H 3), 5.15 (d, 1H, J=9Hz, sugar ring H 1), 5.11-5.24 (m, 2H, sugar ring H 5And H 4), 4.85 (dd, J=3.9Hz, J=9Hz, sugar ring H 2), 4.11-4.24 (m, 2H, sugar ring H 6), 3.75-3.78 (m, 1H, C α AspH), 2.96 (m, 1H, C β Asp H), 2.63-2.69 (m, 1H, AspC β H), 1.97-2.09 (m, 12H, 4 * CH of sugar ring ethanoyl 3), 1.43 (S, 9H, 3 * CH 3), 1.28 (S, 9H, 3 * CH 3). 13CNMR (300MHz, CDCI 3) δ 170.4,170.0,169.2,169.1,168.6,167.6,148.6,133.8,133.2,132.0,131.2,123.5,85.1,82.3,74.3,67.5,81.5,74.0,61.3,69.7,55.9,38.9,27.9,27.5,20.6,20.5,20.49,20.47.
The preparation of embodiment 16N-(2,3,4,5-four-O-ethanoyl-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine di tert butyl carbonate
Operation according to embodiment 15; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 2.1g (5mmol) N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine di tert butyl carbonate; obtain 3.55g (95%) title compound; Rf (cyclohexane/ethyl acetate; 2: 1) be 0.24; mp67-69 ℃, [α] D 20=+28 (C=1.5, CHCI 3).
1H NMR (500MHz, CDCI 3): δ 8.27-8.29 (d, J=8Hz, 1H, pheH 3), 7.6-7.75 (m, 2H, phe H 4With phe H 5), 7.52-7.53 (d, J=5Hz, phe H 6), 5.24-5.28 (m, 1H, sugar ring H 3), 5.16-5.19 (m, 1H, sugar ring H 4), 5.08-5.1 (d, 1H, J=9Hz, sugar ring H 1), 4.45 (m, 1H, cysC α H), 4.19 (dd, J=4Hz, J=12.5Hz, 1H, sugar ring H6), 4.15 (dd, J=2Hz, J=12.5Hz, 1H, sugar ring H6), 3.71-3.73 (d, J=10Hz, 1H, sugar ring H 2), 3.75-3.78 (m, 1H, sugar ring H 5), 3.01-3.05 (m, 1H, cysC β H), 2.75 (m, 1H, cysC β H), 2.01-2.1 (m, 12H, 4 * CH of sugar ring ethanoyl 3), 1.33 (S, 9H, 3 * CH 3), 1.24 (S, 9H, 3 * CH 3). 13N MR (500MHz, CDCI 3) δ 170.48,170.31,169.21,168.5,167.6,148.9,134,133,132,131,123,84,82,74,69.9,69.7,67,61,59.9,69.8,43.1,30.8,20.5.
The preparation of embodiment 17N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate
Operation according to embodiment 15; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 2.22g (5mmol) N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate; obtain 3.68g (95%) title compound; Rf (cyclohexane/ethyl acetate; 2: 1) be 0.26; mp68-70 ℃, [α] D 20=+36 (C=1.1, CHCL 3). 1H NMR (500MHz, CDCI 3) δ 8.27-8.29 (d, J=8Hz, 1H, pheH 3), 7.6-7.75 (m, 2H, phe H 4With phe H 5), 7.52-7.53 (d, J=5Hz, 1H, pheH 6), 5.88 (m, 1H, sugar ring H 2), 5.13-5.32 (m, 2H, sugar ring H 3And H 4), 5.02 (d, 1H, J=9Hz sugar ring H 1), 4.47-4.5 (m.1H, gluC α H), 4.15 (dd, J=4Hz, J=12.5Hz, 1H, sugar ring H 6), 4.28 (dd, J=4Hz, J=12.5Hz, 1H, sugar ring H 6), 3.71-3.75 (m, 1H. sugar ring H 5), 1.83-2.42 (m, 16H, 2 * CH 2, 4 * CH of sugar ring ethanoyl 3), 1.45 (S, 9H, 3 * CH 3), 1.22 (S, 9H, 3 * CH 3). 13C NMR (500MHz, CDCI 3) δ 171.1,170.2,170.0,169.0,168.5,168.3,148.7,134.0,132.6,131.9,131.7,123.1,84.3,82.1,74.2,80.5,69.1,67.1,61.0,58.9,68.5,31.4,27.8,27.3,27.1,20.5,20.4,20.3.
The preparation of embodiment 18N-(2,3,4,5-four-O-ethanoyl-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl
Operation according to embodiment 15; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 2.02g (5mmol) N-(ortho-nitrophenyl alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl; obtain 1.03g (28.2%) N-(2; 3; 4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl and 2.41g (65.8%) N-(2; 3; 4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl.
N-(2,3,4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl: Rf (cyclohexane/ethyl acetate, 2: 1) is 0.24, mp63-65 ℃, [α] D 20=+32 (C=1.2, CHCI 3). 1H NMR (300MHz CDCI 3), δ 8.48-8.51 (d, J=7.5Hz, 1H, phe H 3), 7.59-7.71 (m, 3H, pheH 4, pheH 5, pheH 6), 5.78-5.79 (d, J=3Hz, 1H, sugar ring H 1), 5.58-5.6 (m, 1H, sugar ring H 2), 4.9-5.05 (m, 2H, sugar ring H 3And H 4), 4.95-4.97 (m, 1H, serC α H), 3.96-4.08 (m, 2H, sugar ring H 6), 3.71-3.77 (m, 2H, the CH of ser 2), 3.67-3.69 (m, 1H, sugar ring H 5), 2.00-2.11 (m, 12H, 4 * CH of sugar ring ethanoyl 3), 1.46 (S, 9H, 3 * CH 3), 1.39 (S, 9H, 3 * CH 3).
N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl: Rf (cyclohexane/ethyl acetate, 2: 1) is 0.26, mp 64-65 ℃, [α] D 20=+49 (C=1.5, CHCL 3).
1H NMR (300MHz, CDCI 3) δ 7.49-7.71 (m, 3H, phe H 4, phe H 5And pheH 6), 8.48-8.51 (d, J=7.5Hz, 1H, pheH 3), 5.77-5.80 (t, J=9.3Hz, 1H, sugar ring H 2), 5.38-5.41 (d, J=9.6Hz, 1H, sugar ring H 1) .1-5.26 (m, 2H, sugar ring H 3And H 4), 4.61-4.63 (m, 1H, J=6Hz, serC α H), 4.21 (dd, J=4.8Hz, J=12.5Hz, 1H, sugar ring H 6), 4,1-4.13 (d, J=10.5Hz, 1H, sugar ring H 6), 3.85-3.88 (m, 1H, sugar ring H 5), 3.69-3.77 (m, 2H, β CH 2), 2.01-2.2 (m, 12H, 4 * CH of sugar ring ethanoyl 3), 1.35 (S, 9H, 3 * CH 3), 1.23 (S, 9H, 3 * CH 3).
The preparation of embodiment 19N-(2,3,4,5-four-O-ethanoyl-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester
Operation according to embodiment 15; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 2.03g (5mmol) N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester; obtain 0.71g (19.2%) N-(2; 3; 4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester and 2.83g (76.8%) N-(2; 3; 4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester.
N-(2,3,4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-L-phenylalanine tert-butyl ester: Rf (cyclohexane/ethyl acetate, 2: 1) is 0.22, mp70-71 ℃, [α] D 20=+27 (C=1.2, CHCI 3). 1HNMR (300MHz, CDCI 3), δ 8.12-8.14 (d, J=8.1Hz, 1H, phe H 3), 7.59-7.71 (m, 3H ,-pheH 4, pheH 5And pheH 6), 7.29-7.33 (m, 5H, pheH), 5.75-5.76 (d, J=3Hz, 1H, sugar ring H 1), 5.28 (m, 1H, sugar ring H 2), 4.98-5.05 (m, 1H ,-phe α CH), 4.90-4.98 (m, 2H, sugar ring H 3With sugar ring H 4), 4.36-4.38 (m, 1H, sugar ring H 5), 4.21-4.23 (m, 2H, sugar ring H 6), 3.53-3.56 (d, J=9Hz, 1H, pheC β H), 3.21 (dd, J=1.3Hz, J=3.9Hz pheC β H), 1.98-2.22 (m, 12H, 4 * CH of sugar ring ethanoyl 3), 1.27 (S, 9H, 3 * CH 3).
N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-L-phenylalanine tert-butyl ester: Rf (cyclohexane/ethyl acetate, 2: 1) is 0.24, mp 71-73 ℃, [α] D 20=+50 (C=1.7, CHCL 3). 1HNMR (300MHz CDCI 3) δ 8.22-8.24 (d, J=9.6Hz, 1H, pheH 3), 7.56-7.68 (m, 2H ,-pheH 4And pheH 5), 7.46-7.48 (d, J=6Hz, 1H, pheH 6), 7.29-7.31 (m, 5H, pheH), 5.89 (br s, 1H, sugar ring H 2), 5.17-5.29 (m, 3H, sugar ring H 3, sugar ring H 4,-phe C α H), 4.57-4.6 (d, J=9Hz, 1H, sugar ring H 1), 4.06-4.15 (m, 2H, sugar ring H 6), 3.75 (m, 1H, sugar ring H 5), 2.92-3.13 (m, 2H, the CH of phe 2) .1.95-2.05 (m, 12H, 4 * CH of sugar ring ethanoyl 3) 1.2 (S, 9H, 3 * CH 3).
The preparation of embodiment 20N-(2,3,4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid
760mg (1mmol) N-(2; 3,4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate mixed the back stirring at room 3 hours with the 6.4ml trifluoroacetic acid; TLC (cyclohexane/ethyl acetate, 2: 1) shows that raw material point disappears.Trifluoroacetic acid is removed in decompression, the residue acetone solution, and concentrating under reduced pressure again, so repeatedly, to remove residual trifluoroacetic acid.Residue obtains 583mg (90%) title compound with column chromatography purification (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2), and Rf (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) is 0.19, and mp110-113 ℃, [α] D 20=+67.2 (C=1.5, CHCL 3). 1H NMR (300MHz, CDCI 3) δ 8.74 (S, 2H, 2 * COOH), 8.15-8.18 (m, 1H, pheH 3), 7.71-7.75 (m, 2H, pheH 4, H 6), 7.57-7.6 (m, pheH 5), 5.68 (d, J=2.4Hz, 1H, sugar ring H 1), 5.20 (dd, J=2.4Hz, J=10.1Hz, 1H, sugar ring H 2), 5.10 (t, J=3Hz, 1H, sugar ring H 3) 4.93-4.96 (m, 2H, sugar ring H 4And H 5), 4.32-4.36 (m, 1H, AspC α H), 4.26 (dd; J=4.5Hz, J=12Hz, sugar ring H6), 4.16 (dd; J=5.4Hz, J=12Hz, sugar ring H6), 3.28 (dd; J=10.2Hz, J=16.2Hz, 1H, AspC β H); 2.68 (dd, J=3Hz, J=16.2Hz, 1H; AspC β H), 2.02-2.16 (m, 12H, 4 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 21N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid
According to the operation of embodiment 20, with 760mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 577mg (89%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) is 0.18; mp 95-97 ℃, [α] D 20=+31.5 (C=1.1, CHCI 3). 1H NMR (300MHz, CDCI 3) δ 8.79 (S, 2H, 2 * COOH), 8.25-8.27 (d, J=7.8Hz, pheH 3), 7.57-7.72 (m, 3H, pheH 4.H 5.H 6), 5.55 (m, 1H, sugar ring H 3), 5.15 (d, 1H, J=9Hz, sugar ring H1), 5.11-5.24 (m, 2H, sugar ring H 5And H 4), 4.85 (dd, J=3.9Hz, J=9Hz, sugar ring H 2), 4.11-4.24 (m, 2H, sugar ring H 6), 3.75-3.78 (m, 1H, AspC α H), 2.96 (m, 1H, AspC β H), 2.63-2.69 (m, 1H, AspC β H), 1.97-2.09 (m, 12H, 4 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 22N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine
Operation according to embodiment 20; with 748mg (1mmol) N-(2; 3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-the S-tertiary butyl-N-(ortho-nitrophenyl alkylsulfonyl)-L-halfcystine tert-butyl ester replacement N-(2; 3; 4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 630mg (91%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) is 0.20; mp 93-95 ℃, [α] D 20=+63.4 (C=1.1, CHCI 3), 1H NMR (500MHz, CDCI 3): δ 8.80 (S, 1H, COOH), 8.27-8.29 (d, J=8Hz, 1H, pheH 3), 7.6-7.75 (m, 2H, phe H 4With phe H 5), 7.52-7.53 (d, J=5Hz, phe H 6), 5.85 (m, 1H, sugar ring H 5), 5.24-5.28 (m, 1H, sugar ring H 3), 5.16-5.19 (m, 1H, sugar ring H 4), 5.08-5.1 (d, 1H, J=9Hz, sugar ring H 1), 4.45 (m, 1H, H αCys), 4.19 (dd, J=4Hz, J=12.5Hz, 1H, sugar ring H 6), 4.15 (dd, J=2Hz, J=12.5Hz, 1H, sugar ring H 6), 3.71-3.73 (d, J=10Hz, 1H, sugar ring H 2), 3.01-3.05 (m, 1H, cysC β H), 2.75 (m, 1H, cysC β H), 2.01-2.1 (m, 12H, 4 * CH of sugar ring ethanoyl 3), 1.33 (S, 9H, 3 * CH 3).
The preparation of embodiment 23N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid
According to the operation of embodiment 20, with 774mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-glutamic acid tert-butyl replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 583mg (88%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) is 0.18; mp110-112 ℃, [α] D 20=+49.0 (C=1.1, CHCI 3). 1H NMR (300MHz, CDCI 3) δ 8.81 (S, 2H, 2 * COOH), 8.27-8.29 (d, J=8Hz, 1H, pheH 3), 7.6-7.75 (m, 2H, phe H 4With phe H 5), 7.52-7.53 (d, J=5Hz, 1H, pheH 6), 5.88 (m, 1H, sugar ring H 2), 5.13-5.32 (m, 2H, sugar ring H 3And H 4), 5.02 (d, 1H, J=9Hz sugar ring H 1), 4.47-4.5 (m.1H, gluC α H), 4.15 (dd, J=4Hz, J=12.5Hz, 1H, sugar ring H6), 4.28 (dd, J=4Hz, J=12.5Hz, 1H, sugar ring H6), 3.71-3.75 (m, 1H. sugar ring H 5), 1.83-2.42 (m, 16H, 2 * CH 2, 4 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 24N-(2,3,4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine
According to the operation of embodiment 20, with 732mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 558mg (90%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) is 0.21; mp 90-92 ℃, [α] D 20=+30 (C=1.1, CHCI 3). 1H NMR (300MHzCDCI 3), δ 9.01 (S, 1H, COOH), 8.48-8.51 (d, J=7.5Hz, 1H, phe H 3), 7.59-7.71 (m, 3H, pheH 4, pheH 5And pheH 6), 5.78-5.79 (d, J=3Hz, 1H, sugar ring H 1), 5.58-5.6 (m, 1H, sugar ring H 2), 4.9-5.05 (m, 2H, sugar ring H 3And H 4), 4.95-4.97 (m, 1H, the C α H of ser), 3.96-4.08 (m, 2H, sugar ring H 6), 3.71-3.77 (m, 2H, β CH 2), 3.67-3.69 (m, 1H, sugar ring H 5), 2.00-2.11 (m, 12H, 4 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 25N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine
According to the operation of embodiment 20, with 732mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 570mg (92%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) is 0.23; mp 89-91 ℃, [α] D 20=+7 (C=1.0, CHCL 3). 1H NMR (300MHz, CDCI 3) δ 8.80 (S, 1H, COOH), 8.48-8.51 (d, J=7.5Hz, 1H, pheH 3), 7.49-7.71 (m, 3H, phe H 4, phe H 5And pheH 6), 5.77-5.80 (t, J=9.3Hz, 1H, sugar ring H 2), 5.38-5.41 (d, J=9.6Hz, 1H, sugar ring H 1), 5.10-5.26 (m, 2H, sugar ring H 3And H 4), 4.61-4.63 (m, 1H, J=6Hz, the C α H of Ser), 4.21 (dd, J=4.8Hz, J=12.5Hz, 1H, sugar ring H 6), 4,1-4.13 (d, J=10.5Hz, 1H, sugar ring H 6), 3.85-3.88 (m, 1H, sugar ring H 5), 3.69-3.77 (m, 2H, β CH 2), 2.01-2.2 (m, 12H, 4 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 26N-(2,3,4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine
According to the operation of embodiment 20, with 736mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 626mg (92%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) is 0.29; mp 89-90 ℃, [α] D 20=+66.0 (C=1.9, CHCI 3). 1H NMR (300MHz, CDCI 3), δ 8.12-8.14 (d, J=8.1Hz, 1H, phe H 3), 7.59-7.71 (m, 3H ,-pheH 4, pheH 5And pheH 6), 7.26-7.31 (m, 5H, pheH), 5.75-5.76 (d, J=3Hz, 1H, sugar ring H 1), 5.28 (m, 1H, sugar ring H 2), 4.98-5.05 (m, 1H, the C α H of-phe), 4.90-4.98 (m, 2H, sugar ring H 3With sugar ring H 4), 4.36-4.38 (m, 1H, sugar ring H 5), 4.21-4.23 (m, 2H, sugar ring H 6), 3.53-3.56 (d, J=9Hz, 1H, the CH of phe 2), 3.21 (dd, J=1.3Hz, the CH of J=3.9Hz phe 2), 1.98-2.22 (m, 12H, 4 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 27N-(2,3,4,5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine
According to the operation of embodiment 20, with 736mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 639mg (94%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) is 0.31; mp 77-79 ℃, [α] D 20=+10.0 (C=1.1, CHCI 3). 1H NMR (300MHz CDCI 3), δ 8.81 (S, 1H, COOH), 8.22-8.24 (d, J=9.6Hz, 1H, pheH 3), 7.56-7.68 (m, 2H ,-pheH 4And pheH 5), 7.46-7.48 (d, J=6Hz, 1H, pheH 6), 7.16-7.28 (m, 5H, pheH), 5.89 (br s, 1H, sugar ring H 2), 5.17-5.29 (m, 3H, sugar ring H 3, sugar ring H 4With phe C α H), 4.57-4.6 (d, J=9Hz, 1H, sugar ring H 1), 4.06-4.15 (m, 2H, sugar ring H 6), 3.75 (m, 1H, sugar ring H 5), 2.92-3.13 (m, 2H, the CH of phe 2) .1.95-2.05 (m, 12H, 4 * CH of sugar ring ethanoyl 3).
The system of embodiment 28N-(α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid
648mg (1mmol) N-(2; 3; 4,5-four-O-ethanoyl-α-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl sulfo group)-L-aspartic acid and the 20ml solution that newly steams anhydrous methanol adds 92mg (1.7mmol) sodium methylate under ice bath, makes reaction mixture keep PH 10-11.Reaction mixture stirring at room 24 hours, TLC (petrol ether/ethyl acetate/glacial acetic acid, 2: 1: 0.2) shows that raw material point disappears.Add H in king's reaction mixture +Type ion exchange resin is transferred PH4, filters, and filtrate decompression is concentrated into dried, obtains 384mg (80%) title compound, and Rf (chloroform/methanol/water/glacial acetic acid, 1: 1: 0.2: be 0.18 0.1), mp 152-154 ℃, [α] D 20=+29.3 (C=1.2, CH 3OH), FAB/MS (m/e) 503[M+Na] +..
The preparation of embodiment 29N-(β-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid
According to the operation of embodiment 28, with 648mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid replaces N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 456mg (95%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 1: 1: 0.2: be 0.20 0.1); mp 157-158 ℃, [α] D 20=+8.3 (C=1.2, CH 3OH), FAB/MS (m/e) 503[M+Na] +..
The preparation of embodiment 30N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine
According to the operation of embodiment 28, with 692mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine replacement N-(2,3,4; 5-four-O-ethanoyl α-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 508mg (97%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 1: 1: 0.2: be 0.27 0.1); mp108-110 ℃, [α] D 20=+14.6 (C=1.0, CH 3OH). 1H NMR (500MHz, DMSO-d 6), δ 9.05 (S, 1H, COOH), 8.54-8.55 (d, J=9Hz, 1H, phe H 3), 7.81-7.87 (m, 2H, pheH 4, pheH 5), 7.71-7.74 (t, J=15.5Hz, 1H, pheH 6), 5.16 (d, 1H, J=9Hz, sugar ring H 1), 4.44 (m, 1H, the C α H of-cys), 4.23 (dd, J=5Hz, 10.5Hz, 1H, sugar ring H 2), 3.65-3.67 (d, J=10Hz, 1H, sugar ring H 6), 3.49-3.51 (d, J=10Hz, 1H, sugar ring H 6), 3.4-3.41 (m, 1H, sugar ring H 3), 3.17-3.22 (m, 1H, sugar ring H 4), 3.05-3.1 (m, 1H, sugar ring H 5), 2.76-2.78 (d, J=12Hz, 1H, the C β Hb of cys), 2.52 (br s, 1H, the C β Ha of cys), 1.19 (S, 9H, 3 * CH 3).
The preparation of embodiment 31N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid
According to the operation of embodiment 28, with 662mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 464mg (94%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: be 0.25 0.1); mp 103-105 ℃, [α] D 20=+21.0 (C=1.1, CH 3OH). 1H NMR (500MHz, D 2O), and δ 12.7 (S, 2H, COOH), 8.18-8.20 (d, J=9Hz, 1H, phe H 3), 7.83-7.89 (m, 2H, phe H 4, pheH 5), 7.73-7.75 (t, J=10Hz, 1H, pheH 6),, 5.16 (d, 1H, J=9Hz, sugar ring H 1), 4.42 (m, 1H, the C α H of glu), 3.83 (d, J=12Hz, 1H, sugar ring H 6), 3.59-3.62 (m, 2H, sugar ring H 2AndH 6), 3.52-3.54 (m, 1H, sugar ring H 3), 3.43-3.45 (m, 1H, sugar ring H 5), 3.35-3.37 (m, 1H, sugar ring H 4), 2.16-2.45 (m, 4H, 2 * CH 2).
The preparation of embodiment 32N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine
According to the operation of embodiment 28, with 620mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 416mg (92%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: be 0.27 0.1); mp 100-102 ℃, [α] D 20=-19.6 (C=1.1, CH 3OH). 1H NMR (300MHz, DMSO-d 6), δ 12.5-13 (brS, 1H ,-COOH), 8.48-8.51 (d, J=7.5Hz, 1H, pheH 3), δ 7.49-7.71 (m, 3H, phe H 4, phe H 5And pheH 6), 4.67-4.73 (d, 1H, J=9Hz, sugar ring H 1), 4.39-4.42 (m, 1H ,-SerH a), 3.57-3.61 (m, 2H, sugar ring H 2And sugar ring H 6), 3.57-3.92 (m, 3H, sugar ring H 3, sugar ring H 6With sugar ring H 5), 3,18-3.21 (m, 3H, sugar ring H 4And β CH 2).
The preparation of embodiment 33N-(α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine
According to the operation of embodiment 28, with 620mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 496mg (80%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: be 0.25 0.1); mp 91-94 ℃, [α] D 20=+29 (C=1.1, CH 3OH).Instability is used for next step reaction immediately.
The preparation of embodiment 34N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine
According to the operation of embodiment 28, with 680mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 481mg (94%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: be 0.35 0.1); mp 98-101 ℃, [α] D 20=-21.0 (C=1.1, CH 3OH). 1H NMR (300MHz, DMSO-d 6), δ 8.44-8.47 (d, J=8.1Hz, 1H, pheH 3), 7.77-7.78 (m, 2H ,-pheH 4And pheH 5), 7.65-7.70 (m, 1H, pheH 6), 7.13-7.31 (m, 5H ,-pheH), 4.78-4.81 (d, 1H, J=8.7Hz, sugar ring H 1), 4.55 (m, 1H, the C α H of-phe), 4.38 (dd, J=3.9Hz, 9Hz, 2H, sugar ring CH 2), 3.60-3.69 (m, 3H, sugar ring H 2, sugar ring H 3With sugar ring H 5), 3.4-3.52 (m, 1H, sugar ring H 4), 3.09-3.21 (m, 2H, the CH of phe 2).
The preparation of embodiment 35N-(α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine
According to the operation of embodiment 28, with 681mg (1mmol) N-(2,3; 4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine replacement N-(2,3,4; 5-four-O-ethanoyl-α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 415mg (81%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: be 0.30 0.1); mp 104-106 ℃, [α] D 20=+19.0 (C=1.2, CH 3OH).Unstable products is directly used in next step reaction.
The preparation of embodiment 36N-(1-deoxidation-β-D-fructose-1-yl)-L-aspartic acid
At Ar 2Protection adds 0.7ml (4mmol) diisopropyl ethyl amine and 0.71ml (7mmol) thiophenol down in the solution of 48mg (0.1mmol) N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid and 2ml dry DMF.Reaction mixture is in stirring at room 4 hours, TLC (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: 0.1) show raw material point disappearance.Yellow residue was used the 10ml water dissolution earlier after concentrating under reduced pressure was removed DMF, used the 5ml acetic acid ethyl dissolution again.Acetic acid ethyl acetate extract is washed twice with 2.5ml.The water layer that merges washes twice with the 5ml ethyl acetate, is evaporated to dried then.Residue obtains 25mg (84%) title compound with Sephadex LH20 purifying, is the very strong colorless solid of water absorbability.Rf (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: be 0.22 0.1), [α] D 20=-20.34 (C=1.8, H 2O).TOF/MS(M/Z)：294[M] +。 1H NMR (500MHz, D 2O), δ 3.91 (dd, J=3.3Hz, J=9.8Hz, 1H, sugar ring H 6), 3.78 (dd, J=2Hz, J=12.3Hz, 1H, sugar ring H 6), 3.73 (d, J=10.7Hz, 1H, sugar ring H 4), 3.70 (m, 1H, sugar ring H 5), 3.60-3.61 (d, J=5Hz, 1H, sugar ring H 3), 3.58 (m, 1H ,-aspC α H), 3.41-3.42 (d, J=5Hz, 1H, sugar ring H 1), 3.36-3.38 (d, J=10Hz, 1H, sugar ring H 1), 2.86 (dd, J=4.28Hz, J=10Hz, 1H, AspCH 2), 2.80 (dd, J=7.4Hz, J=15Hz, 1H, AspCH 2). 13C NMR (500MHz, D 2O), δ 174.3 (C=O), 171.8 (C=O) .94.43 (C 2), 74.2 (C 3), 71.29 (C 4), 69.97 (C 5), 68.13 (C 6), 59.1 (AspC α), 52.9 (C 1), 33.4 (AspC β).
The preparation of embodiment 37N-(1-deoxidation-α-D-fructose-1-yl)-L-aspartic acid
Operation according to embodiment 36; replace N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 48mg (0.1mmol) N-(α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 24mg (81%) title compound Rf (chloroform/methanol/water/glacial acetic acid; 2: 1: 0.2: be 0.22 0.1), [α] D 20=-20.34 (C=1.8, H 2O).TOF/MS(M/Z)：294[M] +。 1H NMR (500MHz, D 2O), δ 3.97 (m, 1H, sugar ring H 5), 3.88-3.89 (d, J=5Hz, 1H, sugar ring H 6), 3.77 (dd, J=3.2Hz, J=7.5Hz, 1H, sugar ring H 6), 3.68 (S, 1H, sugar ring H 4), 3.65-3.66 (d, J=5Hz, 1H, sugar ring H 3), 3.58-3.62 (m, 1H, AspC α H), 3.35-3.37 (d, J=10Hz, 1H, sugar ring H 1), 3.22-3.24 (d, J=10Hz, 1H, sugar ring H 1), 2.93-2.97 (m, 2H, Asp β CH 2).
The preparation of embodiment 38N-(1-deoxidation-β-D-fructose-1-yl)-L-L-glutamic acid
Operation according to embodiment 36; replace N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 50mg (0.1mmol) N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid; obtain 27mg (87%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 2: 1: 0.2: be 0.20 0.1), [α] D 20=-52.00 (C=1.0, H 2O).TOF/MS(M/Z)：308[M] +。 1HNMR (500MHz, D 2O), δ 4.01 (dd, J=3.8Hz, J=11.5Hz, 1H, sugar ring H 6), 3.99 (m, 1H, sugar ring H 5), 3.88 (dd, J=4Hz, J=10.5Hz, 1H, sugar ring H 4), 3.76 (dd, J=3.8Hz, J=11.5Hz, 1H, sugar ring H 6), 3.75 (d, J=7Hz, 1H, sugar ring H 3), 3.73 (m, 1H, GluH α), 3.32 (d, J=10Hz, 1H, sugar ring H 1), 3.21 (d, J=10Hz, 1H, sugar ring H 1),, 2.18 (m, 2H, glu β CH 2), 2.58 (m, 2H ,-glu γ CH 2).
The preparation of embodiment 39N-(1-deoxidation-β-D-fructose-1-yl)-L-Serine
Operation according to embodiment 36; replace N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 45mg (0.1mmol) N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine; obtain 23mg (85%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 2: 1: 0.2: be 0.23 0.1), [α] D 20=-35.00 (C=1.2, H 2O).TOF/MS(M/Z)：266[M] +。 1HNMR (500MHz, D 2O), δ 3.96 (dd, J=4Hz, J=10Hz, 1H, sugar ring H 6), 3.92 (d, J=4Hz, 1H, sugar ring H 6), 3.90 (m, 1H, sugar ring H 5), 3.78-3.81 (m, 1H, sugar ring H 4), 3.69-3.70 (d, J=5Hz, 1H, sugar ring H 3), 3.63 (m, 1H, SerC α H), 3.31-3.32 (d, J=5Hz, 1H, sugar ring H 1), 3.10-3.12 (d, J=10Hz, 1H, sugar ring H 1), 3.2 (t, J=10Hz, 1H, SerC β Ha), 3.06 (t, J=10Hz, 1H, SerC β Hb).
The preparation of embodiment 40N-(1-deoxidation-α-D-fructose-1-yl)-L-Serine
Operation according to embodiment 36; replace N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 45mg (0.1mmol) N-(α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine; obtain 17mg (65%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 2: 1: 0.2: be 0.21 0.1), [α] D 20=+7.69 (C=1.3, H 2O).TOF/MS(M/Z)：266[M] +。 1H NMR (500MHz, D 2O), δ 3.23 (br s, 1H, sugar ring H 1), 3.36 (br s, 1H, sugar ring H 1), 3.66 (d, J=10Hz, 1H, sugar ring H 3), 3.77 (dd, J=3.35Hz, J=5Hz, 1H, sugar ring H 4), 3.88 (m, 1H, sugar ring H 5), 3.68 (dd, J=2Hz, J=12Hz, 1H, sugar ring H 6), 3.83 (d, J=2Hz, J=5.5Hz, 1H, sugar ring H 6), 3.71-3.73 (t, J=10Hz, 1H, Ser C α H), 3.89-3.91 (d, J=10Hz, 1H, Ser β C H 2), 3.93 (d, J=15Hz, 1H, Ser β CH 2). 13C NMR (500MHz, D 2O), δ 175.2 (C=O), 99.5 (C 2), 72.76 (C 3), 67.5 (C 4), 66.6 (C 5), 57.6 (C 6), 57.0 (SerC α), 53 (C β), 49 (C 1).
The preparation of embodiment 41N-(1-deoxidation-β-D-fructose-1-yl)-L-phenylalanine
Operation according to embodiment 36; replace N-(β-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 51mg (0.1mmol) N-(β-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine; obtain 26mg (80%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 2: 1: 0.2: be 0.30 0.1), [α] D 20=+130.00 (C=1.4, H 2O).TOF/MS(M/Z)：326[M] +。 1H NMR (500MHz, D 2O) δ 7.19-7.33 (m.5H, pheH), 3.14-3.15 (d, J=5Hz, 1H, sugar ring H 1), 3.16-3.18 (d, J=10Hz, 1H, sugar ring H 1), 3.58-3.59 (d, J=5Hz, 1H, sugar ring H 3), 3.62 (dd, J=1.95Hz, J=11.5Hz, 1H, sugar ring H 4), 3.60 (m, 1H, sugar ring H 5), 3.73 (dd, J=3.3Hz, J=9.8Hz, 1H, sugar ring H 6), 3.85-3.86 (dd, J=3.8Hz, J=9Hz, 1H, sugar ring H 6), 3.62 (m, 1H, phe C α H), 3.1 (d, J=5Hz, 1H, phe β C H 2), 3.6 (d, J=5Hz, 1H, phe β CH 2). 13C NMR (300MHz, D 2O), 175.2 (C=O), 137.4,137.2,131.99,131.92,131.85,130.4 (phe), 55.5 (C 1), 97.77 (C 2), 80.6 (C 5), 72.8 (C 3), 71.9 (C 4), 66.55 (C 6), 66.46 (pheC α), 38.3 (pheC β).
The preparation of embodiment 42N-(1-deoxidation-α-D-fructose-1-yl)-L-phenylalanine
Operation according to embodiment 36; replace N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 51mg (0.1mmol) N-(α-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine; obtain 25mg (75%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 2: 1: 0.2: be 0.28 0.1), [α] D 20=+29 (C=1.1, H 2O).TOF/MS(M/Z)：326[M] +。 1H NMR (500MHz, D 2O), and δ 7.18-7.28 (m, 5H, pheH), 3.18 (d, J=5.56Hz, 1H, sugar ring H 1A), 3.13 (dd, 1H, pheC β Ha), 3.23 (d, J=5.27Hz, 1H, sugar ring H 1B), 3.54 (dd, 1H, pheC β H b), 3.62 (m, 1H, pheC α H), 3.67-3.69 (d, J=10Hz, 1H, sugar ring H 3), 3.85 (m, 1H, sugar ring H 5), 3.87 (dd, J=1.2Hz, J=5Hz, 1H, sugar ring H 4), 3.88 (dd, 1H, sugar ring H 6B), 3.99 (dd, J=2.7Hz, J=10.2Hz, 1H, sugar ring H 6A).
The preparation of embodiment 43N-(1-deoxidation-β-D-fructose-1-yl)-S-tertiary butyl-L-halfcystine
Operation according to embodiment 36; replace N-(β-D-Glucopyranose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 53mg (0.1mmol) N-(β-D-Glucopyranose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine; obtain 30mg (85%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 2: 1: 0.2: be 0.35 0.1); 138 ℃ of mp (decomposition), [α] D 20=-31.00 (C=1.43, C 2H 5OH/H 2O, 1: 10).TOF/MS(M/Z)：338[M] +。
The preparation of embodiment 44N-(1-deoxidation-β-D-fructose-1-yl)-L-halfcystine
Be dissolved in the 2ml glacial acetic acid with 90mg (0.3mmol) N-(1-deoxidation-β-D-fructose-1-yl)-S-tertiary butyl-L-halfcystine, 75mg (0.4mmol) ortho-nitrophenyl sulphinyl chlorine.At Ar 2Under the protection, reaction soln stirring at room 2 hours, TLC (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: 0.1) show that raw material point disappears.The residue that concentrating under reduced pressure obtains is washed till neutrality with ether, uses the 2ml dissolve with methanol then.At ice bath and Ar 2Protection down, gradation adding 80mg (2.2mmol) NaBH in the solution 4Obtained the reaction mixture stirring at room 4 hours.Be evaporated to dried, the residue water dissolution, the aqueous solution that obtains is washed (50 * 3) with ethyl acetate, water layer is evaporated to dried.Residue Sephadex LH 20Column purification with 10% aqueous ethanolic solution wash-out, the fraction lyophilize of collecting, obtains 32mg (43%) title compound, 258 ℃ of mp (decomposition), [α] D 20=-31.00 (C=1.0, H 2O).TOF/MS(M/Z)：301[M] +。 1H NMR (500MHz, D 2O) 3.0 (dd, J=1.25Hz, J=3Hz, 2H, the CH of cys 2), 3.3 (d, J=2.5Hz, 1H, sugar ring H 1A), 3.4 (d, J=2.5Hz, 1H, sugar ring H 1), 3.49 (m, 1H, cysC α H), 3.63 (d, J=2.5Hz, 1H, sugar ring H 3), 3.72 (m, 1H, sugar ring H 4), 3.79 (dd, J=1.25Hz, J=3Hz, 1H, sugar ring H 6), 3.87 (m, 1H, sugar ring H 5), 4.01 (d, J=2.5Hz, 1H, sugar ring H 6).
Embodiment 451,2,3, the preparation of 5-four-O-ethanoyl-D-furans pectinose
4.0g anhydrous sodium acetate is heated to and boils with after 200 diacetyl oxides mix.Stir the adding of gradation inward 15g (0.1mol) D-pectinose down, last 2 hours.Utilize the reaction liberated heat to keep backflow during this time.Reheat refluxed 3 hours afterwards, and the color and luster of reaction mixture becomes palm fibre gradually afterwards.Reaction mixture is cooled to about 60 ℃, in the impouring 100ml frozen water, follows and stir the oily matter in the adding 300ml ethyl acetate extraction frozen water in the frozen water.The separating ethyl acetate layer, water layer extracts (4 * 50ml) again with ethyl acetate.With and ethyl acetate layer, once with the saturated NaCL aqueous solution wash (2 * 50ml), saturated NaHCO 3The aqueous solution wash (2 * 50ml) with the saturated NaCL aqueous solution (20 * 50ml) wash, anhydrous Na SO 4Dry.Filter, filtrate decompression is concentrated into dried, obtains 23.9mg (75%) title compound.Rf (ethyl acetate/petroleum ether 1: 2, is launched twice), the α body is 0.58, and the β body is 0.59, and α/β is 1: 9.
Embodiment 461,2,3, the preparation of 5-four-O-ethanoyl-D-furans pectinose
The mixture of 15g (0.1mol) D-pectinose and 150 diacetyl oxides/pyridine (2: 1) 90-100 ℃ the heating 6 hours after, stirring at room 14 hours.Obtain following stirring in the pale brown colour response liquid impouring 500ml frozen water.After 3 hours, reaction mixture chloroform extraction (3 * 100ml).The organic layer that merges is washed saturated NaHCO with 2N dilute hydrochloric acid 3The aqueous solution is washed, and the saturated NaCL aqueous solution is washed, washing.The anhydrous MgSO of organic layer 4, to filter, filtrate decompression is concentrated into dried, obtains 28.6g (90%) title compound, and α: β is 1: 1.
Embodiment 472,3, the preparation of 5-three-O-ethanoyl-D-furans pectinose
Add 6ml (90mmol) quadrol in the new 150ml anhydrous tetrahydro furan that steams, add 5.3ml (90mmol) glacial acetic acid under the stirring at room, adularescent smog overflows.The mixture stirring at room adds 1,2,3 of embodiment 45 preparations, 5-four-O-ethanoyl-D-furans pectinose 15.9g (50mmol), restir 14 hours after 30 minutes.TLC (ethyl acetate/petroleum ether, 1: 2) shows that raw material point disappears.Reaction mixture is evaporated to dried, and residue obtains 12.4g (90%) title compound with column chromatography purification (ethyl acetate/petroleum ether, 1: 2), and Rf (ethyl acetate/petroleum ether, 1: 2) is 0.31.
Embodiment 482,3, the preparation of 5-three-O-ethanoyl-D-furans pectinose
According to the operation of embodiment 47, with 1,2 of embodiment 46 preparations; 3,5-four-O-ethanoyl-D-furans pectinose 15.9g (50mmol) replaces 1,2 of embodiment 45 preparations; 3,5-four-O-ethanoyl-D-furans pectinose obtains 12.3g (89%) title compound.
The preparation of embodiment 49N-(2,3,5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate
The 552mg (2mmol) 2 of embodiment 47 preparations; 3; 5-three-O-ethanoyl-D-furans pectinose, 524mg (2mmol) triphenylphosphine, 430mg (1mmol) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate and 15ml newly steam the solution of anhydrous tetrahydro furan at Ar 2Under the protection ,-80 ℃ are stirred the quick 0.39ml (2mmol) of adding diisopropyl azodiformate after 15 minutes.Reaction mixture slowly is warming up to room temperature, lasts 2 hours.The reaction mixture stirring at room is the disappearance of TLC (ethyl acetate/petroleum ether, 1: 2) demonstration raw material point after 14 hours.Reaction mixture is evaporated to dried; residue separates with silica gel medium pressure H post; obtain 509mg (74%) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate and 145mg (21.1%) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate.
N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.22, [α] D 20=+49.6 (C=1.1, CHCI 3). 1H NMR (500MHz, CDCI 3) δ 7.58-7.60 (m, 1H, pheH 6), 7.67-7.70 (m, 2H, pheH 4, pheH 5), 8.24-8.25 (d, J=9.5Hz, 1H, pheH 3), 5.22-5.23 (t, J=6.5Hz, 1H, sugar ring H 1), 5.02-5.04 (dd, J=3.5Hz, J=10Hz, 1H, sugar ring H 2), 4.92-4.95 (q, J=13.5Hz, 1H, sugar ring H 4), 4.04 (dd, J=3Hz, J=13Hz, 1H, sugar ring H 3), 3.68-3.71 (d, J=13.5Hz, 1H, sugar ring H 5), 3.02-3.04 (m, 1H, aspC α H), 2.75 (dd, J=4.5Hz, J=15Hz, 1H, sugar ring H 5), 2.2 (s, 3H, the CH of sugar ring ethanoyl 3), 2.17 (s, 3H, the CH of sugar ring ethanoyl 3), 2.14 (m, 2H, AspCH 2), 2.00 (s, 3H, the CH of sugar ring ethanoyl 3), 1.45 (S, 9H, 3 * CH 3), 1.32 (S, 9H, 3 * CH 3).
N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.24, [α] D 20=+8.0 (C=1.3, CHCI 3). 1H NMR (500MHz, CDCI 3) δ 8.16 (dd, J=3.5Hz, J=5.75Hz, 1H, pheH 3), 7.57-7.59 (m, 1H, pheH 6), 7.74-7.76 (m, 2H, pheH 4And pheH 5), 5.51 (br s, 1H, sugar ring H 1), 5.29-5.3 (t, J=5.5Hz, 1H, sugar ring H 2), 5.20-5.23 (dd, J=2.5Hz, J=10.5Hz, 1H, sugar ring H 5), 5.12-5.16 (m, 1H, sugar ring H 4), 4.95-4.98 (m, 1H, aspC α H), 4.81 (br.S, 1H, sugar ring H 3), 3.88-3.90 (dd, J=1Hz, J=10.5Hz, 1H, sugar ring H 5), 3.91-3.95 (dd, J=5.5Hz, J=15Hz, 1H, aspCH 2), 3.21-3.26 (dd, J=10.5Hz, J=17Hz, 1H, aspCH 2), 2-2.2 (s, 9H, sugar ring ethanoyl 3 * CH 3), 1.46 (S, 9H, 3 * CH 3), 1.32 (S, 9H, 3 * CH 3).
The preparation of embodiment 50N-(2,3,5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester
Operation according to embodiment 49; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 418mg (1mmol) N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester; obtain 383mg (56.7%) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester and 191mg (28.3%) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester.
N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.23, mp 66-67 ℃, [α] D 20=+50.0 (C=1.1, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 7.54-7.56 (d, J=7.5Hz, 1H, pheH 6), 7.65-7.72 (m, 2H, pheH 4And pheH 5), 8.26-8.27 (d, J=8Hz, pheH 3), 5.26 (br s, 1H, sugar ring H 1), 5.04 (dd, J=3.5Hz, J=11.5Hz, 1H, sugar ring H 2), 4.93 (m, 2H, sugar ring H 4With cysC α H), 4.42-4.45 (m, 1H, sugar ring H 3), 4-4.03 (d, J=15Hz, 1H, sugar ring H 5), 3.64-3.66 (d, J=10Hz, 1H, sugar ring H 5), 3.1 (t, J=10Hz, 1H, cysCH 2), 2.76 (S, 1H, cysCH 2), 2.02-2.2 (s, 9H, sugar ring ethanoyl 3 * CH 3), 1.23 (S, 9H, 3 * CH 3), 1.34 (S, 9H, 3 * CH 3). 13C NMR (500MHz, CDCI 3), δ 170.3,170,168.6,167.6 (C=O), 148.8,133.7,132.9,131.8,131,123.4 (aromatic carbon), 82.4,72.2 (2 tC tBu), 85.3,68.2,67.8,66,60 (sugar ring carbon), 66.4 (cysC α), 42.9 (cysC β) 30.7,27.4,27.3,21.8,20.8,20.7,20.57,20.5 (saturated carbon).
N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.25, mp 70-71 ℃, [α] D 20=+10.0 (C=1.1, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 7.57-7.59 (m, 1H, pheH 6), 7.73-7.75 (m, 1H, pheH4 and pheH5), 8.2-8.22 (m, 1H, pheH 3), 5.55 (s, 1H, sugar ring H 1), 5.31-5.33 (t, J=7Hz, 1H, sugar ring H 2), 5.06-5.1 (m, 1H, sugar ring H 4), 4.83-4.84 (d, J=3.5Hz, 1H, sugar ring H 3), 4.68-4.71 (dd, J=4.5Hz, J=8.8Hz, 1H, sugar ring H 5), 3.93-3.95 (m, 1H, cysC α H), 3.93-3.94 (d, J=3.5Hz, 1H, sugar ring H 5), 3.41-3.48 (m, 1H, cysCH 2), 2.76 (dd, J=4.5Hz, J=15Hz, 1H, cysCH 2) .1.98-2.15 (s, 9H, 3 * CH of sugar ring ethanoyl 3), 1.31 (S, 9H, 3 * CH of the tertiary butyl 3), 1.47 (S, 9H, 3 * CH of the tertiary butyl 3). 13C NMR (500MHz, CDCI 3), δ 169.7,169.2, and 168.8,168.3 (C=O), 148.8,134.3,132.3,131.9,131.4,123.5 (fragrant C), 80.7 (tertiary carbons of the tertiary butyl), 83.3,70.7,66.5,63.9, (61.8 sugar ring carbon), 66.4 (cysC α), 42.6 (cysC β), 30.7,30.4,27.6,21,20 (saturated carbon).
The preparation of embodiment 51N-(2,3,5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate
Operation according to embodiment 49; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 444mg (1mmol) N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate; obtain 477mg (67.9%) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate and 159mg (22.6%) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-glutamic acid tert-butyl.
N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.21, mp73-75 ℃, [α] D 20=+45.0 (C=1.2, CHCI 3).
1H NMR (500MHz, CDCI 3), δ 7.51-7.53 (d, J=7.5Hz, 1H, pheH 6), 7.62-7.69 (m, 2H, pheH 4, pheH 5), 8.23-8.25 (d, J=8Hz, pheH 3), 6.03 (br S, 1H, sugar ring H 3), 5.23 (s, 1H, sugar ring H 1), 5.0 (dd, J=3.5Hz, J=9.5Hz, 1H, sugar ring H 2), 4.78-4.81 (br s, 1H, sugar ring H 4), 4.46-4.49 (t, J=15Hz, 1H, gluC α H), 3.96 (dd, J=1.5Hz, J=13.5Hz, 1H, sugar ring H 5), 3.58-3.61 (d, J=13Hz, 1H, sugar ring H 5), 2.33-2.36 (m, 2H, γ CH 2), 2.08-2.12 (m, 2H, β CH 2), 2.01-2.22 (S, 9H, 3 * CH of sugar ring ethanoyl 3), 1.19 (S, 9H, 3 * CH of the tertiary butyl 3), 1.44 (S, 9H, 3 * CH of the tertiary butyl 3).
N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.23, mp 71-73 ℃, [α] D 20=+15.0 (C=1.2, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 7.53-7.55 (m, 1H, pheH 6), 7.69-7.73 (m, 1H, pheH 4, pheH 5), 8.08-8.09 (m, 1H, pheH 3), 5.5 (d, J=1.5Hz, 1H, sugar ring H 1), 5.36 (br s, 1H, sugar ring H 2), 4.98-5.02 (m, 1H, sugar ring H 4), 4.92 (br.s, 1H, sugar ring H 3), 4.61-4.64 (m, 1H, gluC α H), 3.85-3.91 (m, 2H, sugar ring H 5), 2.34-2.55 (m, 2H, γ CH 2), 2.2-2.25 (m, 2H, β CH 2), 1.96 (S, 9H, 3 * CH of sugar ring ethanoyl 3), 1.42-1.43 (S, 18H, 6 * CH of the tertiary butyl 3).
The preparation of embodiment 52N-(2,3,5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl
Operation according to embodiment 49; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 402mg (1mmol) N-(ortho-nitrophenyl alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl; obtain 501mg (76%) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl and 125mg (19%) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl.
N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.23, mp 61-63 ℃, [α] D 20=-+82.2 (C=1.1, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 8.3-8.32 (d, J=10Hz, pheH 3), 7.62-7.65 (m, 2H, pheH 4, pheH 5), 7.51-7.52 (d, J=9Hz, pheH 6), 5.95 (S, 1H, sugar ring H 1), 5.25 (br s, 1H, sugar ring H 2), 5.2-5.21 (d, J=5Hz, 1H, sugar ring H 4), 4.99 (dd, J=3.5Hz, J=9.5Hz, 1H, sugar ring H 3), 4.5 (m, 1H, serC α H), 4.01-4.04 (dd, J=1Hz, J=10.5Hz, 1H, sugar ring H 5), 3.7-3.82 (m, 2H, serCH 2), 3.63-3.66 (d, J=14.5Hz, 1H, sugar ring H 5), 1.99,2.03,2.19 (S, 9H, 3 * CH of sugar ring ethanoyl 3), 1.17 (S, 9H, 3 * CH of the tertiary butyl 3), 1.25 (S, 9H, 3 * CH of the tertiary butyl 3). 13CNMR (500MHz, CDCI 3), 170.4,170.1,168.6,167.7 (C=O), 148.5,133.5,132.3,131.1,123.2 (aromatic carbons), 81.7,73.7 (tertiary carbons of the tertiary butyl), 86.6,72.2,68.2,67,62 (sugar ring carbon) .68.5,60.6 (serC α and C β), 27.5,27.2,20.98,20.8,20.6 (saturated C).
N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.24, mp 58-62 ℃, [α] D 20=+7.0 (C=1.2, CHCI 3). 1HNMR (500MHz, CDCI 3), δ 8.51-8.52 (d, J=7.5Hz, 1H, pheH 3), 7.65-7.7 (m, 3H, pheH 4, pheH 5, pheH 6), 5.38 (m, 1H, sugar ring H 2), 5.35 (S, 1H, sugar ring H 1), 5.1-5,14 (m, 1H, sugar ring H 4), 4.98-4.99 (d, J=4Hz, 1H, sugar ring H 3), 4.64-4.67 (m, 1H, serC α H), 4.04 (dd, J=5Hz, J=10Hz, 1H, sugar ring H 5), 3.96 (dd, J=5.5Hz, J=10.8Hz, 1H, sugar ring H 5), 3.7-3.77 (m, 2H, CH 2), 1.96-2.12 (S, 9H, 3 * CH of sugar ring ethanoyl 3), 1.15 (S, 9H, 3 * CH 3), 1.45 (S, 9H, 3 * CH 3). 13CNMR (500MHz, CDCI 3), δ 169.6,168.9,168.7,168.6 (C=O), 133.6,131.8,130.8,124, (123.1 aromatic carbon), 81.3,73.5 (tertiary carbons of the tertiary butyl), 83.3,70.8,66.38,61.3,64.0 (sugar ring carbon), 64.2,61.4 (serC α and C β), 27.6,27.4,21.8,21.1,20.67,20.60 (saturated C).
The preparation of embodiment 53N-(2,3,5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester
Operation according to embodiment 49; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 406mg (1mmol) N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester; obtain 493mg (74.2%) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester and 100mg (15%) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester.
N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-L-phenylalanine tert-butyl ester: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.24, mp 75-77 ℃, [α] D 20=+14.8 (C=1.0, CHCI 3).
1H NMR (500MHz, CDCI 3), δ 7.54-7.56 (d, 1H, pheH 6), 7.65-7.7 (m, 2H, pheH 4, pheH 5), 8.29 (dd, J=1.5Hz, J=4.2Hz, pheH 3), 7.27-7.29 (m, 5H, phe), 6.01 (br s, 1H, sugar ring H 1), 5.29-5.31 (br s, 1H, sugar ring H 2), 5.11 (dd, J=3.5Hz, J=10Hz, 2H, sugar ring H 4With sugar ring H 3), 4.57-4.59 (m, 1H, pheC α H), 4.04 (dd, J=2Hz, J=10Hz, 1H, sugar ring H 5), 3.69-3.71 (d, J=13Hz, 1H, sugar ring H 5), 3.23 (m, 1H, pheCH 2), 3.02-3.06 (m, 1H, pheCH 2), 2.01-2.199 (S, 9H, 3 * CH of sugar ring ethanoyl 3), 1.26 (S, 9H, 3 * CH of the tertiary butyl 3). 13C NMR (500MHz, CDCI 3), δ 170.2,169.9,168.7,167.9 (C=O), 148,77,133.8,131.5,131.3,131.15,129.35,129,128.2,126.7, (123.3 aromatic carbon), 81.6 (tertiary butyl C-O), 85.2,72.04,68.1,67.5,60.7 (sugar ring carbon), 66.2 (pheC α), 38.5,27.1,26.9,21.6,20.7,20.5,20.4 (saturated carbon).
N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-L-phenylalanine tert-butyl ester: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.25, mp 68-70 ℃, [α] D 20=+44.4 (C=1.1, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 8.17-8.18 (d, J=8Hz, pheH 3), 7.69-7.64 (m, 2H, pheH 4, pheH 5), 7.59-7.60 (d, J=7.5Hz, 1H, pheH 6), 7.3-7.33 (m, 5H ,-C 6H 5), 5.63 (s, 1H, sugar ring H 1), 5.35 (t, 1H, sugar ring H 2), 5.18-5.21 (m, 1H, pheC α H), 4.89-4.92 (m, 2H, sugar ring H 3With sugar ring H 4), 3.94-4 (m, 2H, sugar ring H 5), 3.59 (dd, J=10Hz, J=13.5Hz, 1H, pheCH 2), 3.11-3.14 (d, J=13.5Hz, 1H, pheCH 2), 1.99,2.17 (S, 9H, 3 * CH of sugar ring ethanoyl 3), 1.39 (S, 9H, 3 * CH 3). 13C NMR (500MHz, CDCI 3), δ 169.7,169.2,168.9,168.3 (C=O), 148.7,139.3,134.3,132.3,131.8,131.2,128.9,128.1,126.2, (123.4 aromatic carbon), 81 (tertiary butyl C-O), 82.7,70.7,66.4,64.02,61.4 (sugar ring carbon), 64.1 (pheC α), (39.2 pheC β), 27.5,20.5,20.8 (saturated carbon).
The preparation of embodiment 54N-(2,3,5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-threonine tert-butyl ester
Operation according to embodiment 49; replace N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate with 416mg (1mmol) N-(ortho-nitrophenyl alkylsulfonyl)-O-tertiary butyl-L-threonine tert-butyl ester; obtain 488mg (72.4%) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-threonine tert-butyl ester and 125mg (18.6%) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-threonine tert-butyl ester.
N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-threonine tert-butyl ester: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.26, mp 77-79 ℃, [α] D 20=+6.0 (C=1.0, CHCI 3).
1H NMR (300MHz, CDCI 3), δ 8.36-8.39 (m, 1H, pheH 3), 7.59-7.68 (m, 2H, pheH 4And pheH 5), 7.53-7.56 (m, 1H, pheH 6), 6.14-6.21 (t, J=19.5Hz, 1H,, sugar ring H 4), 5.39-5.43 (d, J=12Hz, 1H,, sugar ring H 1), 5.23-5.24 (d, J=2.7Hz, 1H,, sugar ring H 2), 4.92 (dd, J=3.3Hz, J=10.2Hz, 1H,, sugar ring H 3), 4.5 (d, J=3Hz, 1H, thrC α H), 4.31-4.34 (m, 1H, thrC β H), 3.82-3.86 (d, J=13.2Hz, 1H,, sugar ring H 5) 3.57-3.61 (d, J=13.5Hz, 1H,, sugar ring H 5), 2.01 (S, 9H, 3 * CH 3), 2.09 (S, 9H, 3 * CH 3), 2.21 (S, 9H, 3 * CH 3), 1.33-1.35 (d, J=6Hz, 3H, CH 3), 1.30 (S, 9H, 3 * CH 3), 1.17 (S, 9H, 3 * CH 3). 13C NMR (500MHz CDCI 3), 170.4,170.1,168.6,167.3 (C=O), 148.6,134.6,133.4,132.8,131.05, (123.4 aromatic carbon), 81.7,74.1 (tertiary carbons of the tertiary butyl), 87.4,73.2,69.4,65.2,68.9 (sugar ring carbon), 67.1 (thrC α), (68.7 thrC β), 31.6,28.7,27.8,21.1,21,20.6,19.4 (saturated carbon).
N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-O-tertiary butyl-L-threonine tert-butyl ester: Rf (ethyl acetate/petroleum ether, 1: 2) is 0.27, mp 73-75 ℃, [α] D 20=+64.0 (C=1.0, CHCI 3). 1H NMR (300MHz, CDCI 3), δ 8.26-8.29 (m, 1H, pheH 3), 7.56-7.72 (m, 3H, pheH 4, pheH 5, pheH 6), 5.76 (d, J=1.2Hz, 1H, sugar ring H 1), 5.43 (t, J=6.3Hz, 1H, sugar ring H 4), 5.27 (dd, J=5Hz, J=14.4Hz, 1H, sugar ring H 2), 5.14 (d, J=3Hz, 1H, sugar ring H 3), 4.26-4.29 (m, 1H, thrC α H), 4.5 (t, J=16.2Hz, 1H, thrC β H), 3.96-3.98 (d, J=8.1Hz, 2H, sugar ring H 5), 1.80-1.82 (d, J=6.6Hz, 3H, CH 3), 1.96-2.17 (S, 9H, 3 * CH of sugar ring ethanoyl 3), 1.52 (S, 9H, the tertiary butyl 3 * CH 3), 1.37 (S, 9H, the tertiary butyl 3 * CH 3). 13C NMR (300MHz, CDCI 3), 169.7,169.5,168.8,168.1, (C=O), 148,134.6,133.4,132.8,131.0,123.4 (aromatic carbons), 81.7,74.4 (tertiary carbons of the tertiary butyl), 83.6,70.1,68.5,67,63.9 (sugar ring carbon), 64.6 (thrC α), (71.7 thrC β), 34.4 (thrC r), 29.1,27.8,21.1,21.0,21.6,19.4 (saturated carbon).
The preparation of embodiment 55N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid
688mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate and 5.5ml trifluoroacetic acid stirring at room 3 hours; TLC (ethyl acetate/petroleum ether; 1: 2) show that raw material point disappears, the reaction mixture concentrating under reduced pressure, residue is evaporated to dried with acetone solution again; residual trifluoroacetic acid is removed in this operation repeatedly.Residue obtains 530mg (92%) title compound with column chromatography purification (petrol ether/ethyl acetate/glacial acetic acid, 1: 1: 0.2), and Rf (petrol ether/ethyl acetate/glacial acetic acid, 1: 1: 0.2) is 0.15, and mp 113-115 ℃, [α] D 20=+89.3 (C=1.0, CHCI 3). 1H NMR (500MHz, CDCI 3) δ 8.72 (S, 2H, 2 * COOH), δ 8.16 (dd, J=3.5Hz, J=5.75Hz, 1H, pheH 3), 7.57-7.59 (m, 1H, pheH 6), 7.74-7.76 (m, 2H, pheH 4And pheH 5), 5.51 (br s, 1H, sugar ring H 1), 5.29-5.3 (t, J=5.5Hz, 1H, sugar ring H 2), 5.20-5.23 (dd, J=2.5Hz, J=10.5Hz, 1H, sugar ring H 5), 5.12-5.16 (m, 1H, sugar ring H 4), 4.95-4.98 (m, 1H, aspC α H), 4.81 (br.S, 1H, sugar ring H 3), 3.88-3.90 (dd, J=1Hz, J=10.5Hz, 1H, sugar ring H 5), 3.91-3.95 (dd, J=5.5Hz, J=15Hz, 1H, aspCH 2), 3.21-3.26 (dd, J=10.5Hz, J=17Hz, 1H, aspCH 2), 2-2.2 (s, 9H, 3 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 56N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid
Operation according to embodiment 55; with 688mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate replaces N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate to obtain 489mg (90%) title compound; Rf (petrol ether/ethyl acetate/glacial acetic acid; 1: 1: 0.2) be 0.18, mp 110-113 ℃, [α] D 20=+25.3 (C=1.0, CHCI 3). 1HNMR (500MHz, CDCI 3) δ 8.72 (br s, 2H ,-COOH), 7.58-7.60 (m, 1H, pheH 6), 7.67-7.70 (m, 2H, pheH 4, pheH 5), 8.24-8.25 (d, J=9.5Hz, 1H, pheH 3), 5.22-5.23 (t, J=6.5Hz, 1H, sugar ring H 1), 5.02-5.04 (dd, J=3.5Hz, J=10Hz, 1H, sugar ring H 2), 4.92-4.95 (q, J=13.5Hz, 1H, sugar ring H 4), 4.04 (dd, J=3Hz, J=13Hz, 1H, sugar ring H 3), 3.68-3.71 (d, J=13.5Hz, 1H, sugar ring H 5A), 3.02-3.04 (m, 1H, aspC α H), 2.75 (dd, J=4.5Hz, J=15Hz, 1H, sugar ring H 5B), 2.2 (s, 3H, the CH of sugar ring ethanoyl 3), 2.17 (s, 3H, the CH of sugar ring ethanoyl 3), 2.14 (m, 2H, AspCH 2), 2.00 (s, 3H, the CH of sugar ring ethanoyl 3).
The preparation of embodiment 57N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid
Operation according to embodiment 55; with 702mg (1mmol) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate replacement N-(2,3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 543mg (92%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 1: 1: 0.2) is 0.22; mp 96-98 ℃, [α] D 20=+14.0 (C=1.1, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 8.97 (S, 2H, COOH), 7.53-7.55 (m, 1H, pheH 6), 7.69-7.73 (m, 1H, pheH 4, pheH 5), 8.08-8.09 (d, J=5Hz, 1H, pheH 3), 5.45 (d, J=1.5Hz, 1H, sugar ring H 1), 5.38 (br s, 1H, sugar ring H 2), 4.98-5.07 (m, 1H, sugar ring H 4), 4.96 (br.s, 1H, sugar ring H 3), 4.61-4.64 (m, 1H, gluC α H), 3.89-3.94 (m, 2H, sugar ring H 5), 2.44-2.65 (m, 2H, glu γ CH 2), 2.2-2.25 (m, 2H, glu β CH 2), 1.96-2.18 (S, 9H, 3 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 58N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid
Operation according to embodiment 55; with 702mg (1mmol) N-(2; 3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid di tert butyl carbonate replacement N-(2,3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 531mg (90%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 1: 1: 0.2) is 0.20; mp 117-119 ℃, [α] D 20=+94.0 (C=1.1, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 8.97 (S, 2H, COOH), 7.51-7.53 (d, J=7.5Hz, 1H, pheH 6), 7.62-7.69 (m, 2H, pheH 4, pheH 5), 8.23-8.25 (d, J=8Hz, pheH 3), 5.97 (br S, 1H, sugar ring H 3), 5.13 (s, 1H, sugar ring H 1), 5.0 (dd, J=3.5Hz, J=9.5Hz, 1H, sugar ring H 2), 4.68-4.71 (br s, 1H, sugar ring H 4), 4.36-4.45 (t, J=15Hz, 1H, gluC α H), 3.96 (dd, J=1.5Hz, J=13.5Hz, 1H, sugar ring H 5), 3.58-3.61 (d, J=13Hz, 1H, sugar ring H 5), 2.53-2.56 (m, 2H, glu γ CH 2), 2.08-2.12 (m, 2H, glu β CH 2), 2.01-2.22 (S, 9H, 3 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 59N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine
Operation according to embodiment 55; with 664mg (1mmol) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester replacement N-(2,3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 535mg (88%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 1: 1: 0.2) is 0.23; mp 98-101 ℃, [α] D 20=+6.6 (C=1.1, CHCI 3), 1H NMR (500MHz, CDCI 3), δ 8.74 (S, 1H, COOH), 8.17-8.18 (d, J=8Hz, pheH 3), 7.69-7.64 (m, 2H, pheH 4, pheH 5), 7.59-7.60 (d, J=7.5Hz, 1H, pheH 6), 7.21-7.29 (m, 5H ,-C 6H 5), 5.66 (s, 1H, sugar ring H 1), 5.29 (t ,=10Hz, 1H, sugar ring H 2), 5.18-5.21 (m, 1H, pheC α H), 4.89-4.92 (m, 2H, sugar ring H 3With sugar ring H 4), 3.94-4 (m, 2H, sugar ring CH 2), 3.57 (dd, J=10Hz, J=13.5Hz, 1H, pheCH 2), 3.11-3.14 (d, J=13.5Hz, 1H, pheCH 2), 2.17 (S, 3H, the CH of sugar ring ethanoyl 3), 2.05 (S, 3H, the CH of sugar ring ethanoyl 3), 1.89 (S, 3H, the CH of sugar ring ethanoyl 3).
The preparation of embodiment 60N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine
Operation according to embodiment 55; with 664mg (1mmol) N-(2; 3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine tert-butyl ester replacement N-(2,3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 565mg (93%) title compound, Rf (petrol ether/ethyl acetate/glacial acetic acid, 1: 1: 0.2) is 0.27; mp 117-119 ℃, [α] D 20=+85.2 (C=1.1, CHCI 3). 1HNMR (500MHz, CDCI 3), δ 8.69 (S, 1H, COOH), 7.54-7.56 (d, 1H, pheH 6), 7.65-7.7 (m, 2H, pheH 4, pheH 5), 8.29 (dd, J=1.5Hz, J=4.2Hz, pheH 3), 7.27-7.29 (m, 5H, pheH), 5.99 (br s, 1H, sugar ring H 1), 5.27-5.31 (br s, 1H, sugar ring H 2), 5.11 (dd, J=3.5Hz, J=10Hz, 2H, sugar ring H 4With sugar ring H 3), 4.51-4.59 (m, 1H, pheC α H), 4.04 (dd, J=2Hz, J=10Hz, 1H, sugar ring H 5), 3.69-3.71 (d, J=13Hz, 1H, sugar ring H 5), 3.23 (m, 1H, pheCH 2), 3.02-3.06 (m, 1H, pheCH 2), 2.01-2.199 (S, 9H, sugar ring ethanoyl 3 * CH 3).
The preparation of embodiment 61N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine
Operation according to embodiment 55; with 660mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl replacement N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 488mg (89%) title compound; Rf (petrol ether/ethyl acetate/glacial acetic acid; 1: 1: 0.2) be 0.21; mp 109-111 ℃, [α] D 20=+9.0 (C=1.1, CHCI 3). 1HNMR (500MHz, CDCI 3), δ 8.77 (S, 1H, COOH), 8.51-8.52 (d, J=7.5Hz, 1H, pheH 3), 7.65-7.7 (m, 3H, pheH 4, pheH 5, pheH 6), 5.48 (m, 1H, sugar ring H 2), 5.35 (S, 1H, sugar ring H 1), 5.1-5,14 (m, 1H, sugar ring H 4), 4.98-4.99 (d, J=4Hz, 1H, sugar ring H 3), 4.64-4.67 (m, 1H, serC α H), 4.04 (dd, J=5Hz, J=10Hz, 1H, sugar ring H 5), 3.96 (dd, J=5.5Hz, J=10.8Hz, 1H, sugar ring H 5), 3.7-3.77 (m, 2H, serCH 2), 1.96-2.12 (S, 9H, 3 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 62N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine
Operation according to embodiment 55; with 628mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-O-tertiary butyl-L-serine tert-butyl replacement N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 503mg (88%) title compound; Rf (petrol ether/ethyl acetate/glacial acetic acid; 1: 1: 0.2) be 0.23; mp 106-109 ℃, [α] D 20=+83.2 (C=1.0, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 8.89 (S, 1H, COOH), 8.3-8.32 (d, J=10Hz, pheH 3), 7.62-7.65 (m, 2H, pheH 4, pheH 5), 7.51-7.52 (d, J=9Hz, pheH 6), 5.95 (S, 1H, sugar ring H 1), 5.25 (br s, 1H, sugar ring H 2), 5.2-5.21 (d, J=5Hz, 1H, sugar ring H 4), 4.99 (dd, J=3.5Hz, J=9.5Hz, 1H, sugar ring H 3), 4.5 (m, 1H, serC α H), 4.01-4.04 (dd, J=1Hz, J=10.5Hz, 1H, sugar ring H 5A), 3.7-3.82 (m, 2H, CH 2), 3.63-3.66 (d, J=14.5Hz, 1H, sugar ring H 5B), 1.99,2.03,2.19 (S, 9H, 3 * CH of sugar ring ethanoyl 3).
The preparation of embodiment 63N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Threonine
Operation according to embodiment 55; with 642mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-O-tertiary butyl-L-threonine tert-butyl ester replacement N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 556mg (95%) title compound; Rf (petrol ether/ethyl acetate/glacial acetic acid; 1: 1: 0.2) be 0.25; mp 103-105 ℃, [α] D 20=+67.0 (C=1.0, CHCI 3). 1H NMR (300MHz, CDCI 3), δ 8.65 (S, 1H, COOH), 8.36-8.39 (m, 1H, pheH 3), 7.59-7.68 (m, 2H, pheH 4And pheH 5), 7.53-7.56 (m, 1H, pheH 6), 6.12-6.21 (t, J=19.5Hz, 1H,, sugar ring H 4), 5.39-5.43 (d, J=12Hz, 1H,, sugar ring H 1), 5.34 (d, J=2.7Hz, 1H,, sugar ring H 2), 4.92 (dd, J=3.3Hz, J=10.2Hz, 1H,, sugar ring H 3), 4.5 (d, J=3Hz, 1H, thrC α H), 4.31-4.34 (m, 1H, thrC β H), 3.82-3.86 (d, J=13.2Hz, 1H,, sugar ring H 5), 3.57-3.61 (d, J=13.5Hz, 1H,, sugar ring H 5), 2.01 (S, 3H, the CH of sugar ring ethanoyl 3), 2.09, (S, 3H, the CH of sugar ring ethanoyl 3), 2.21 (S, 3H, the CH of sugar ring ethanoyl 3), 1.33-1.35 (d, J=6Hz, 3H, CH 3).
The preparation of embodiment 64N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine
Operation according to embodiment 55; with 676mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester replacement N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 570mg (92%) title compound; Rf (petrol ether/ethyl acetate/glacial acetic acid; 1: 1: 0.2) be 0.29; mp 102-105 ℃, [α] D 20=+8.0 (C=1.0, CHCI 3). 1H NMR (500MHz, CDCI 3), δ 8.91 (S, 1H, COOH), 7.57-7.59 (m, 1H, pheH 6), 7.73-7.75 (m, 1H, pheH4 and pheH5), 8.2-8.22 (m, 1H, pheH 3), 5.55 (s, 1H, sugar ring H 1), 5.31-5.33 (t, J=7Hz, 1H, sugar ring H 2), 5.06-5.1 (m, 1H, sugar ring H 4), 4.83-4.84 (d, J=3.5Hz, 1H, sugar ring H 3), 4.70 (dd, J=4.5Hz, J=8.8Hz, 1H, sugar ring H 5), 3.93-3.95 (m, 1H, cysC α H), 3.93-3.94 (d, J=3.5Hz, 1H, sugar ring H 5), 3.41-3.48 (m, 1H, cysCH 2), 2.76 (dd, J=4.5Hz, J=15Hz, 1H, cysCH 2) .1.98-2.15 (s, 9H, 3 * CH of sugar ring ethanoyl 3), 1.47 (S, 9H, 3 * CH of the S-tertiary butyl 3).
The preparation of embodiment 65N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine
Operation according to embodiment 55; with 676mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine tert-butyl ester replacement N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid di tert butyl carbonate; obtain 539mg (87%) title compound; Rf (petrol ether/ethyl acetate/glacial acetic acid; 1: 1: 0.2) be 0.27; mp 117-120 ℃, [α] D 20=+101.0 (C=1.0, CHCI 3). 1HNMR (500MHz, CDCI 3), δ 8.79 (S, 1H, COOH), 7.54-7.56 (d, J=7.5Hz, 1H, pheH 6), 7.65-7.72 (m, 2H, pheH 4And pheH 5), 8.26-8.27 (d, J=8Hz, 1H, pheH 3), 5.26 (br s, 1H, sugar ring H 1), 5.00 (dd, J=3.5Hz, J=11.5Hz, 1H, sugar ring H 2), 4.93 (m, 2H, sugar ring H 4With cysC α H), 4.42-4.45 (m, 1H, sugar ring H 3), 4-4.03 (d, J=15Hz, 1H, sugar ring H 5), 3.64-3.66 (d, J=10Hz, 1H, sugar ring H 5), 3.1 (t, J=10Hz, 1H, cysCH 2), 2.76 (S, 1H, cysCH 2), 2.02-2.2 (s, 9H, sugar ring ethanoyl 3 * CH 3), 1.34 (S, 9H, 3 * CH 3).
The preparation of embodiment 66N-(α-D-pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid
576mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-and N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid and 15ml newly steam anhydrous methanol and add 70.2mg (1.3mmol) sodium methylate with ice bath cooling back, and the pH value that makes reaction mixture is 9-10.Remove ice bath, reaction mixture stirring at room 5 hours, TLC (chloroform/methanol/water/glacial acetic acid, 3: 1: 0.15: 0.1) show that raw material point disappears.In reaction mixture, add H +Type ion exchange resin makes reaction mixture PH transfer to 4.Filter, filtrate decompression is concentrated into dried, obtains 432mg (96%) title compound, and Rf (chloroform/methanol/water/glacial acetic acid, 3: 1: 0.15: be 0.28 0.1), mp 128-130 ℃, [α] D 20=+97.0 (C=1.0, CH 3OH).FAB/MS(m/e)473[M+Na] +。
The preparation of embodiment 67N-(β-D-pectinose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid
Operation according to embodiment 66; with 576mg (1mmol) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid replacement N-(2,3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 364mg (81%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 3: 1: 0.15: be 0.30 0.1); mp134-136 ℃, [α] D 20=+11.0 (C=1.0, CH 3OH) FAB/MS (m/e) 473[M+Na] +
The preparation of embodiment 68N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine
Operation according to embodiment 66; with 620mg (1mmol) N-(2; 3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine replacement N-(2,3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 459mg (93%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 3: 1: 0.15: be 0.31 0.1); mp 127-129 ℃, [α] D 20=+90.0 (C=1.0, CH 3OH).FAB/MS(m/e)517[M+Na] +。
The preparation of embodiment 69N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl the alkylsulfonyl)-S-tertiary butyl-L-halfcystine
Operation according to embodiment 66; with 620mg (1mmol) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine replacement N-(2,3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 395mg (80%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 3: 1: 0.15: be 0.32 0.1); mp 129-131 ℃, [α] D 20=+10.0 (C=1.1, CH 3OH).FAB/MS(m/e)517[M+Na] +。
The preparation of embodiment 70N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid
Operation according to embodiment 66; with 590mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid replacement N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 418mg (90%) title compound; Rf (chloroform/methanol/water/glacial acetic acid 3: 1: 0.15: be 0.29 0.1), mp 117-119 ℃, [α] D 20=+105 (C=1.0, CH 3OH).FAB/MS(m/e)487[M+Na] +。
The preparation of embodiment 71N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid
Operation according to embodiment 66; with 590mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid replacement N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 380mg (82%) title compound; Rf (chloroform/methanol/water/glacial acetic acid 3: 1: 0.15: be 0.31 0.1), mp 108-110 ℃, [α] D 20=+21.0 (C=1.2, CH 3OH).FAB/MS(m/e)487[M+Na] +。
The preparation of embodiment 72N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine
Operation according to embodiment 66; with 548mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine replacement N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 388mg (92%) title compound; Rf (chloroform/methanol/water/glacial acetic acid 3: 1: 0.15: be 0.27 0.1), mp 105-108 ℃, [α] D 20=+39.0 (C=1.2, CH 3OH), FAB/MS (m/e) 445[M+Na] +
The preparation of embodiment 73N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine
Operation according to embodiment 66; with 548mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine replacement N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 354mg (84%) title compound; Rf (chloroform/methanol/water/glacial acetic acid 3: 1: 0.15: be 0.29 0.1), mp110-112 ℃, [α] D 20=+4.5 (C=1.2, CH 3OH), FAB/MS (m/e) 445[M+Na] +
The preparation of embodiment 74N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine
Operation according to embodiment 66; with 608mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine replacement N-(2,3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 448mg (93%) title compound; Rf (chloroform/methanol/water/glacial acetic acid 3: 1: 0.15: be 0.27 0.1), mp123-125 ℃, [α] D 20=+53.0 (C=1.2, CH 3OH), FAB/MS (m/e) 505[M+Na] +
The preparation of embodiment 75N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine
Operation according to embodiment 66; with 608mg (1mmol) N-(2; 3; 5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine replacement N-(2; 3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl) N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid, obtain 386mg (80%) title compound; Rf (chloroform/methanol/water/glacial acetic acid 3: 1: 0.15: be 0.29 0.1), mp113-115 ℃ [α] D 20=+19.0 (C=1.0, CH 3OH), FAB/MS (m/e) 505[M+Na] +
The preparation of embodiment 76N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Threonine
Operation according to embodiment 66; with 562mg (1mmol) N-(2; 3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Threonine replacement N-(2,3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 414mg (95%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 3: 1: 0.15: be 0.21 0.1); mp113-115 ℃, [α] D 20=+87.0 (C=1.2, CH 3OH).FAB/MS(m/e)459[M+Na] +。
The preparation of embodiment 77N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Threonine
Operation according to embodiment 66; with 562mg (1mmol) N-(2; 3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Threonine replacement N-(2,3; 5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 349mg (80%) title compound, Rf (chloroform/methanol/water/glacial acetic acid, 3: 1: 0.15: be 0.23 0.1); mp 101-103 ℃, [α] D 20=+9.0 (C=1.1, CH 3OH).FAB/MS(m/e)459[M+Na] +。
The preparation of embodiment 78N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-aspartic acid
The solution of 45mg (0.1mmol) N-(α-D-pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid and 2mlDMF is at Ar 2Protection adds 0.70ml diisopropyl ethyl amine and 0.71ml thiophenol down.Reaction mixture stirring at room 4 hours, TLC (chloroform/methanol/water/glacial acetic acid, 1: 1: 0.2: 0.1) show that raw material point disappears.The reaction mixture concentrating under reduced pressure is removed and is DMF, and residue is used the 15ml deionized water dissolving earlier, uses the 5ml acetic acid ethyl dissolution again.(2 * 10ml), the ethyl acetate layer water extracts (3 * 5ml) to water layer with ethyl acetate extraction.With and water layer and be evaporated to dried, residue SephadexLH20 column chromatography purification, 10% aqueous ethanolic solution wash-out, collect suitable cut, concentrating under reduced pressure obtains 18.6mg (70%) title compound, be buff syrup shape thing, Rf (chloroform/methanol/water/glacial acetic acid, 1: 1: 0.2: be 0.21 0.1), [α] D 20=+7.55 (C=1.1, H 2O), TOF/MS (M/Z): 264[M] + 1H NMR (500MHz, D 2O), δ 4.37 (m, 1H, sugar ring H 4), 4.14-4.15 (d, J=5Hz, 1H, sugar ring H 3), 4.07 (dd, J=4.5Hz, 12.5Hz, 1H, sugar ring H 5), 3.80-3.84 (m, 1H, sugar ring H 5), 3.34-3.37 (d, J=12.5Hz, 1H, sugar ring H 1), 3.14-3.17 (d, J=12.5Hz, 1H, sugar ring H 1), 3.79-3.85 (m, 1H, C α AspH), 2.63-2.68 (m, 2H, C β AspH). 13CNMR (500MHz, D 2O), δ 177.0,176.0, (C=O), 97,78,71.8,72.2,50.3, (sugar ring carbon) 61.4 (C α), 36.1 (C β).
The preparation of embodiment 79N-(1-deoxidation-β-D-ketofuranose-1-yl)-L-aspartic acid
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 45mg (0.1mmol) N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid; obtain 18.0mg (68%) title compound; be pale brown sugar colour slurry; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.23 0.1), [α] D 20=-20.9 (C=1.1, H 2O), TOF/MS (M/Z): 264[M] +
The preparation of embodiment 80N-(1-deoxidation-α-D-ketofuranose-1-yl)-S-tertiary butyl-L-halfcystine
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 49mg (0.1mmol) N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine; obtain 28.7mg (93%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.25 0.1), [α] D 20=+38.0 (C=1.1, H 2O), TOF/MS (M/Z): 308[M] +
The preparation of embodiment 81N-(1-deoxidation-β-D-ketofuranose-1-yl)-S-tertiary butyl-L-halfcystine
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 46mg (0.1mmol) N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-S-tertiary butyl-L-halfcystine; obtain 19.5mg (71%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.28 0.1), [α] D 20=-16.0 (C=1.0, H 2O), TOF/MS (M/Z): 308[M] +
The preparation of embodiment 82N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-L-glutamic acid
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 46mg (0.1mmol) N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid; obtain 20.9mg (75%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.22 0.1), [α] D 20=+10.0 (C=1.0, H 2O), TOF/MS (M/Z): 278[M] + 1H NMR (500MHZ, D 2O) δ 3.26-3.29 (d, J=13Hz, 1H, sugar ring H 1), 3.15-3.17 (d, J=7.5Hz, 1H, sugar ring H 1), 4.15-4.16 (d, J=4.5Hz, 1H, sugar ring H 3), 4.37 (m, 1H, sugar ring H 4), 4.06 (dd, J=4Hz, J=10Hz, 1H, sugar ring H 5), 3.80 (dd, J=2.7Hz, J=9.8Hz, 1H, sugar ring H 5), 3.85 (m, 1H, gluC α H), 2.0 (m, 2H, glu β CH 2).
The preparation of embodiment 83N-(1-deoxidation-β-D-ketofuranose-1-yl)-L-L-glutamic acid
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 46mg (0.1mmol) N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-L-glutamic acid; obtain 17.5mg (63%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.30 0.1), [α] D 20=-9.0 (C=1.0, H 2O), TOF/MS (M/Z): 278[M] + 1H NMR (500MHZ, D 2O) δ 3.65 (d, J=6.6Hz, 1H, sugar ring H 1), 4.25 (d, J=5Hz, 1H, sugar ring H 1), 3.63 (d, J=7Hz, 1H, sugar ring H 3), 3.54 (dd, J=7Hz, J=14Hz, 1H, sugar ring H 5), 3.36-3.40 (m, 2H, gluC α H and sugar ring H 4), 3.14 (d, J=14.9Hz, 1H, sugar ring H 5), 2.04 (m, 2H, rCH 2), 2.0 (m, 2H, β CH 2).
The preparation of embodiment 84N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-Serine
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 42mg (0.1mmol) N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine; obtain 18.0mg (76%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.28 0.1), [α] D 20=+20.0 (C=1.1, H 2O), TOF/MS (M/Z): 236[M] + 1HNMR (500MHz, D 2O) δ 4.34-4.36 (m, 1H, sugar ring H 4), 4.19 (d, J=4.55Hz, 1H, sugar ring H 3), 4.04 (dd, J=4.7Hz, J=10.2Hz, 1H, sugar ring H 5), 3.83 (m, 1H, C α SerH), 3.82-3.83 (d, J=5.7Hz, 1H, sugar ring H 5), 3.71-3.72Hz (d, J=5.4Hz, 1H, sugar ring H 1), 3.45-3.47 (d, J=8.2Hz, 1H, sugar ring H 1), 3.55-3.57 (m, 2H, β-CH 2).
The preparation of embodiment 85N-(1-deoxidation-β-D-ketofuranose-1-yl)-L-Serine
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 42mg (0.1mmol) N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Serine; obtain 17.1mg (72%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.30 0.1), [α] D 20=-19.0 (C=1.1, H 2O), TOF/MS (M/Z): 236[M] + 1H NMR (500MHz, D 2O) δ 3.65-3.7 (m, 1H, sugar ring H 4), 3.45 (dd, J=6.5Hz, J=11.5Hz, 2H, sugar ring H 5), 3.52 (d, J=4.3Hz, 1H, sugar ring H 3), 3.88-3.89 (d, J=3.94Hz, 1H, sugar ring H 1), 3.54-3.55 (d, J=4.3Hz, 1H, sugar ring H 1), 3.59-3.63 (m, 1H, serC α H), 3.54 (dd, J=4.3Hz, J=11.7Hz, 2H, serCH 2).
The preparation of embodiment 86N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-phenylalanine
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 48mg (0.1mmol) N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine; obtain 23.5mg (79%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.35 0.1), [α] D 20=+6.7 (C=1.2, H 2O), TOF/MS (M/Z): 296[M] + 1H NMR (5O0MHZ, D 2O) (ArH), (sugar encircles H to 4.23-4.24 to δ 7.19-7.30 for m, 1H for m, 5H 4), 4.08-4.09 (d, J=3.55Hz, 1H, sugar ring H 3), 3.87 (dd, J=2.68Hz, J=10.21Hz, 1H, sugar ring H 5), 3.67 (d, J=10.16Hz, 1H, sugar ring H 5), 3.86 (m, 1H, PheC α H), 3.82 (d, J=3.87Hz, 1H, PheC H 2), 3.24-3.26 (d, J=7.5Hz, 1H, sugar ring H 1), 3.15 (m, 1H, PheC H 2), 2.97-2.99 (d, J=10Hz, 1H, sugar ring H 1).
The preparation of embodiment 87N-(1-deoxidation-β-D-ketofuranose-1-yl)-L-phenylalanine
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 48mg (0.1mmol) N-(β-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-phenylalanine; obtain 18.7mg (63%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.37 0.1), [α] D 20=-11.0 (C=1.2, H 2O), TOF/MS (M/Z): 296[M] + 1H NMR (500MHZ, D 2O) δ 3.15-3.17 (d, J=10Hz, 1H, sugar ring H 1), 3.15-3.17 (d, J=8Hz, 1H, sugar ring H 1), 3.99-4.01 (d, J=10Hz, 1H, sugar ring H 3), 4.22 (m, 1H, sugar ring H 4), 3.85 (dd, J=3Hz, J=11Hz, 1H, sugar ring H 5), 3.65 (d, J=11Hz, 1H, sugar ring H 5), 3.67 (m, 1H, phe C α H), 3.58 (d, J=4Hz, 1H, pheC H 2), 3.14 (d, J=6.6Hz, 1H, pheC H 2).
The preparation of embodiment 88N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-Threonine
Press the operation of embodiment 78; replace N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-aspartic acid with 44mg (0.1mmol) N-(α-D-furans pectinose-1-yl)-N-(ortho-nitrophenyl alkylsulfonyl)-L-Threonine; obtain 18.8mg (75%) title compound; Rf (chloroform/methanol/water/glacial acetic acid; 1: 1: 0.2: be 0.27 0.1), [α] D 20=+8.0 (C=1.0, H 2O), TOF/MS (M/Z): 250[M] + 1HNMR (500MHz, D 2O) δ 4.21-4.24 (m, 1H, sugar ring H 4), 4.14-4.16 (d, J=6.5Hz, 1H, sugar ring H 3), 3.9-3.98 (m, 1H, sugar ring H 5), 3.80-3.81 (m, 1H, sugar ring H 5), 3.57-3.59 (d, J=5.7Hz, 1H, sugar ring H 1), 3.49-3.3.51 (d, J=6.8Hz, 1H, sugar ring H 1), 4.11-4.13 (m, 1H, ThrC α H), 3.55-3.56 (m, 1H, ThrC β H), 1.23 (d, J=6.7Hz, 3H ,-CH 3).
The preparation of embodiment 89N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-halfcystine
Be dissolved in the 2ml glacial acetic acid with 31mg (0.1mmol) (1-deoxidation-α-D-ketofuranose-1-yl)-S-tertiary butyl-L-halfcystine, 25mg (0.1mmol) ortho-nitrophenyl sulphinyl chlorine.At Ar 2Under the protection, reaction soln stirring at room 2 hours, TLC (chloroform/methanol/water/glacial acetic acid, 2: 1: 0.2: 0.1) show that raw material point disappears.The residue that concentrating under reduced pressure obtains is washed till neutrality with ether, uses the 2ml dissolve with methanol then.At ice bath and Ar 2Protection down, gradation adding 16mg (0.7mmol) NaBH in the solution 4Obtained the reaction mixture stirring at room 4 hours.Be evaporated to dried, the residue water dissolution, the aqueous solution that obtains is washed (50 * 3) with ethyl acetate, water layer is evaporated to dried.Residue Sephadex LH 20Column purification with 10% aqueous ethanolic solution wash-out, the fraction lyophilize of collecting, obtains 11mg (43%) title compound, 243 ℃ of mp (decomposition), [α] D 20=+10.00 (C=1.1, H 2O).TOF/MS(M/Z)：252[M] +。 1H NMR (500MHz, D 2O), 4.32 (br, S, 1H, sugar ring H 4), 4.17-4.18 (d, 1H, J=4Hz, sugar ring H 3), 4.57 (dd, J=4Hz, J=10Hz, 2H, sugar ring H 5), 3.81 (m, 1H, cysC α H), 3.23-3.25 (d, J=10Hz, 1H, sugar ring H 1), 3.09-3.11 (d, J=10Hz, 1H, sugar ring H 1), 3.07-3.09 (m, 1H, cysCH 2), 2.88-2.92 (m, 1H, cysCH 2).
The preparation of embodiment 90N-(1-deoxidation-β-D-ketofuranose-1-yl)-L-halfcystine
Press the operation of embodiment 89, replace N-(1-deoxidation-α-D-ketofuranose-1-yl)-S-tertiary butyl-L-halfcystine with 31mg (0.1mmol) N-(β-D-furans pectinose-1-yl)-S-tertiary butyl-L-halfcystine, obtain 18.8mg (75%) title compound, yield 32%, mp201 ℃
Figure C20031010042600411
TOFMS [M] +=252, 1HNMR (500MHz, D 2O) δ 3.80 (dd, J=4.2Hz, J=10Hz, 1H, sugar ring H 3), 3.04 (dd, J=4.2Hz, J=10Hz, 2H, sugar ring H 5), 3.03 (d, J=4Hz, 1H, sugar ring H 1), 3.10-3.11 (d, J=5Hz, sugar ring H 1), 3.37 (m, 1H, sugar ring H 4), 3.58-3.61 (m, 1H, cysC α H), 2.90 (dd, J=7.7Hz, J=13.9Hz, cys β CH 2).
Embodiment 91 preparation of compositions
The compounds of this invention 150mg, Magnesium Stearate 10mg, lactose 200mg, starch 140mg tablet producing technology routinely makes tablet.
The foundation of embodiment 92 animal models
Get body weight and be 100 of the healthy Kunming male mices of 20-25g, by per kilogram of body weight 8.2mg dosage abdominal injection Pb (CH 3COO) 23H 2O, inject seven days continuously after, laboratory animal is divided into 10 groups at random, 10 every group.
The selection of embodiment 93 administering modes and dosage
All animals begin intraperitoneal injection after the 48hr that stops to contaminate, positive controls and administration group are all by 0.4mmol/kg (being dissolved in the 0.2ml deionized water) abdominal injection, blank group injection 0.9% physiological saline, positive controls injection DL-Trolovol, administration group Glucoamino acid series is selected N-(1-deoxidation-β-D-fructose-1-yl)-L-aspartic acid (6a β) for use, N-(1-deoxidation-β-D-fructose-1-yl)-L-halfcystine (6b β), N-(1-deoxidation-β-D-fructose-1-yl)-L-phenylalanine (6e β), N-(1-deoxidation-β-D-fructose-1-yl)-L-Serine (6d β), N-(1-deoxidation-β-D-fructose-1-yl)-L-L-glutamic acid (6c β), N-(1-deoxidation-α-D-fructose-1-yl)-L-phenylalanine (6e α); Pectinose series is selected N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-aspartic acid (6a α) for use, N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-halfcystine (6b α), N-(1-deoxidation-α-D-ketofuranose-1-yl)-L-phenylalanine (6e α), N-(1-deoxidation-α-D-ketofuranose-1-base-L-Threonine (6f α).
Embodiment 94 sample collections
After the administration every day 2hr, begin to collect urine within the mouse 5hr; Administration was collected stool in mice in second day as fecal sample the day before yesterday.Continue 5 days, every day 1 group of mouse urine, excrement as a sample.After the last administration 24hr, mouse is taken off neck put to death, observe internal organ and change, separation is also taken out liver, kidney, left side femur and brain as sample.
Embodiment 95 sample process
All biological specimens are all used HNO 3: HCLO 4(3: 1) are nitrated on hot plate to be occurred to the adularescent solid, with the high purity water dissolving and be transferred to constant volume in the volumetric flask, with the plumbous content of Varian spectrAA40 atomic absorption spectrophotometer (graphite furnace method).
Embodiment 96 data processing
Plumbous concentration in the atomic absorption spectrophotometer institute test sample basis is carried out data processing, calculate lead content in every gram sample (urine is lead content in every milliliter of sample), carry out variance analysis.Typical curve r value is between 0.9934-0.9983.
The drive row result of embodiment 97 glucopyranosyl amino acid series medicines
Drive row effect according to the glucopyranosyl amino-acid compound of this name of time-and-motion study of embodiment 92-96, the content of the lead in each tissue (μ g lead/g tissue) is listed table 1 in, plumbous content (μ g lead/g excrement or urine) is listed table 2. result in and is shown that the glucopyranosyl amino-acid compound of this name has good drive row effect in excrement and the urine.
Plumbous content (X ± SE μ g/g) during table 1 mouse is organized after the treatment of glucopyranosyl amino acid
Figure C20031010042600431
A) with Pb+0.9%saline ratio, P＜0.05; B) with Pb+0.9%saline ratio, P＜0.01; C) with Pb+0.9%saline ratio, P＜0.001; D). with Pb+DL-PA ratio, P＜0.01; E). with Pb+DL-PA ratio, P＜0.001; N=10.
Table 2 mouse is plumbous content (X ± SE μ g/g) in excrement and urine after the treatment of glucopyranosyl amino acid
Figure C20031010042600432
A) with Pb+0.9%saline ratio, P＜0.05; B) with Pb+0.9%saline ratio, P＜0.01; C) with Pb+0.9%saline ratio, P＜0.001; D). with Pb+DL-PA ratio, P＜0.05; N=10.
Embodiment 98 arabinofuranosyl amino acid series medicine drive row results
Drive row effect according to the arabinofuranosyl amino-acid compound of this name of time-and-motion study of embodiment 92-96, the content of the lead in each tissue (μ g lead/g tissue) is listed table 3 in, plumbous content (μ g lead/g excrement or urine) is listed table 4. result in and is shown that the arabinofuranosyl amino-acid compound of this name has good drive row effect in excrement and the urine.
Plumbous content (X ± SE μ g/g) during table 3 mouse is organized after the treatment of arabinofuranosyl amino acid
Figure C20031010042600441
A) with Pb+0.9%saline ratio, P＜0.05; B) with Pb+0.9%saline ratio, P＜0.01; C) with Pb+0.9%saline ratio, P＜0.001; D). with Pb+DL-PA ratio, P＜0.05; E). with Pb+DL-PA ratio, P＜0.001; N=10.
Table 4 mouse plumbous content (X ± SE μ g/g) in excrement and the urine after arabinofuranosyl amino acid treatment
A) with Pb+0.9%saline ratio, P＜0.05; B) with Pb+0.9%saline ratio, P＜0.01; C) with
The Pb+0.9%saline ratio, P＜0.001; D). with Pb+DL-PA ratio, P＜0.05; E). with Pb+DL-PA ratio, P＜0.01; N=10.

Claims (9)

1. following general formula (I), (II), (III) or glycosyl amino acid (IV) or its pharmacologically acceptable salts:
Figure C2003101004260002C1
Wherein, R is CH 2COOH, CH 2SH, CH 2CH 2COOH, CH 2OH, CH 2C 6H 5Or CH (OH) CH 3
2. be used to prepare claim 1 formula of (I), (II), (III) or (IV) the amino acid whose intermediate of glycosyl, it is selected from following logical formula V, (VI), (VII) and (VIII)
Figure C2003101004260002C2
Figure C2003101004260003C1
Wherein, R is CH 2COOH, CH 2SH, CH 2CH 2COOH, CH 2OH, CH 2C 6H 5Or CH (OH) CH 3
3. general formula of claim 1 (I) or the amino acid whose preparation method of glycosyl (II) comprise:
A, allow the reaction of the L-amino acid tert-butyl ester and ortho-nitrophenyl SULPHURYL CHLORIDE, make N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
B, allowing the reaction of D-glucose and glacial acetic acid, make 2,3,4,6-O-is tetra-acetylated-the D-Glucopyranose;
C, 2,3,4,6-four-O-ethanoyl-D-Glucopyranose and N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester reaction makes epimerization blended N-2,3,4, the 6-four-O-ethanoyl-D-Glucopyranose-1-base-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
D, obtain N-2 through separation, 3,4,6-four-O-ethanoyl-α-D-Glucopyranose-1-base-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid the tert-butyl ester and N-2,3,4, the 6-four-O-ethanoyl-β-D-Glucopyranose-1-base-N-ortho-nitrophenyl alkylsulfonyl-1-amino acid tert-butyl ester;
E, the α that obtains and beta isomer be deprotection respectively, makes general formula (I) or glycosyl amino acid (II).
4. general formula of claim 1 (III) or the amino acid whose preparation method of glycosyl (IV) comprise:
A, allow the reaction of the L-amino acid tert-butyl ester and ortho-nitrophenyl SULPHURYL CHLORIDE, make N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
B, allow the reaction of D-pectinose and glacial acetic acid, make 2,3,5-three-O-ethanoyl-D-furans pectinose;
C, 2,3,5-three-O-ethanoyl-D-furans pectinose and N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester reaction makes epimeric blended N-(2,3,5-three-O-ethanoyl-D-furans pectinose-1-yl)-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
D, obtain N-(2 through chromatographic separation, 3,5-three-O-ethanoyl-α-D-furans pectinose-1-yl)-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester and N-(2,3,5-three-O-ethanoyl-β-D-furans pectinose-1-yl)-N-ortho-nitrophenyl alkylsulfonyl-L-amino acid tert-butyl ester;
E, the α that obtains and beta isomer deprotection make general formula (III) or glycosyl amino acid (IV).
5. the described general formula of claim 1 (I), (II), (III) or glycosyl amino acid (IV) treat and/or prevent purposes in the medicine of heavy metal poisoning in preparation.
6. according to the purposes of claim 5, wherein heavy metal comprises cadmium, mercury, lead, antimony or arsenic.
7. the described general formula of claim 1 (I), (II), (III) or glycosyl amino acid (IV) purposes in the medicine of preparation row's heavy metal.
8. according to the purposes of claim 7, wherein heavy metal comprises cadmium, mercury, lead, antimony or arsenic.
9. the described general formula of claim 1 (I), (II), (III) that contain significant quantity are or/and the amino acid whose pharmaceutical composition of glycosyl (IV).
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