NO133805B - - Google Patents
Download PDFInfo
- Publication number
- NO133805B NO133805B NO155414A NO15541464A NO133805B NO 133805 B NO133805 B NO 133805B NO 155414 A NO155414 A NO 155414A NO 15541464 A NO15541464 A NO 15541464A NO 133805 B NO133805 B NO 133805B
- Authority
- NO
- Norway
- Prior art keywords
- betaine
- water
- salt
- acid
- carboxylate
- Prior art date
Links
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 64
- 229960003237 betaine Drugs 0.000 claims description 32
- 150000003839 salts Chemical class 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 6
- 150000007530 organic bases Chemical class 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- 239000012736 aqueous medium Substances 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 229910017604 nitric acid Inorganic materials 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 238000000746 purification Methods 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 13
- 239000000243 solution Substances 0.000 description 11
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 10
- 238000002425 crystallisation Methods 0.000 description 7
- 230000008025 crystallization Effects 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- -1 carboxylate anion Chemical class 0.000 description 5
- 229920001429 chelating resin Polymers 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 150000002576 ketones Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000012296 anti-solvent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000006073 displacement reaction Methods 0.000 description 3
- 238000002329 infrared spectrum Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- HOKIDJSKDBPKTQ-GLXFQSAKSA-M cephalosporin C(1-) Chemical compound S1CC(COC(=O)C)=C(C([O-])=O)N2C(=O)[C@@H](NC(=O)CCC[C@@H]([NH3+])C([O-])=O)[C@@H]12 HOKIDJSKDBPKTQ-GLXFQSAKSA-M 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000004108 freeze drying Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- NTEQBPLNPCQJRN-UHUGOGIASA-N 1-[[(6r)-8-oxo-7-[(2-thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]pyridin-1-ium-4-carboxylate Chemical compound C1=CC(C(=O)[O-])=CC=[N+]1CC1=CN2C(=O)C(NC(=O)CC=3SC=CC=3)[C@H]2SC1 NTEQBPLNPCQJRN-UHUGOGIASA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- HOKIDJSKDBPKTQ-GLXFQSAKSA-N Cephalosporin C Natural products S1CC(COC(=O)C)=C(C(O)=O)N2C(=O)[C@@H](NC(=O)CCC[C@@H](N)C(O)=O)[C@@H]12 HOKIDJSKDBPKTQ-GLXFQSAKSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XFTIKWYXFSNCQF-UHFFFAOYSA-N N,N-dipropylformamide Chemical compound CCCN(C=O)CCC XFTIKWYXFSNCQF-UHFFFAOYSA-N 0.000 description 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 238000004279 X-ray Guinier Methods 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000012045 crude solution Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229940071870 hydroiodic acid Drugs 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- NZMAJUHVSZBJHL-UHFFFAOYSA-N n,n-dibutylformamide Chemical compound CCCCN(C=O)CCCC NZMAJUHVSZBJHL-UHFFFAOYSA-N 0.000 description 1
- BNODIVYXTGTUPS-UHFFFAOYSA-N n,n-dimethylpentanamide Chemical compound CCCCC(=O)N(C)C BNODIVYXTGTUPS-UHFFFAOYSA-N 0.000 description 1
- MBHINSULENHCMF-UHFFFAOYSA-N n,n-dimethylpropanamide Chemical compound CCC(=O)N(C)C MBHINSULENHCMF-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J11/00—Devices or arrangements of selective printing mechanisms, e.g. ink-jet printers or thermal printers, for supporting or handling copy material in sheet or web form
- B41J11/26—Pin feeds
- B41J11/32—Adjustment of pin wheels or traction elements, e.g. laterally
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
- A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41L—APPARATUS OR DEVICES FOR MANIFOLDING, DUPLICATING OR PRINTING FOR OFFICE OR OTHER COMMERCIAL PURPOSES; ADDRESSING MACHINES OR LIKE SERIES-PRINTING MACHINES
- B41L5/00—Autographic registers or like manifolding apparatus using movable strips or webs
- B41L5/04—Autographic registers or like manifolding apparatus using movable strips or webs with mechanisms for feeding webs or for arranging web feed; with web storage arrangements
- B41L5/06—Autographic registers or like manifolding apparatus using movable strips or webs with mechanisms for feeding webs or for arranging web feed; with web storage arrangements by means of rollers, wheels, or chains, e.g. with pins transversely
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T403/00—Joints and connections
- Y10T403/59—Manually releaseable latch type
- Y10T403/599—Spring biased manipulator
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T74/00—Machine element or mechanism
- Y10T74/20—Control lever and linkage systems
- Y10T74/20576—Elements
- Y10T74/20636—Detents
- Y10T74/2066—Friction
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Handling Of Sheets (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB43441/63A GB1101561A (en) | 1963-11-04 | 1963-11-04 | Cephalosporin betaines |
| GB4731663 | 1963-12-02 | ||
| GB2885764 | 1964-07-13 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO133805B true NO133805B (pt) | 1976-03-22 |
| NO133805C NO133805C (pt) | 1976-06-30 |
Family
ID=27258760
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO155414A NO133805C (pt) | 1963-11-04 | 1964-11-04 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US3280118A (pt) |
| JP (1) | JPS5021530B1 (pt) |
| BE (2) | BE641338A (pt) |
| CH (2) | CH471078A (pt) |
| CY (1) | CY555A (pt) |
| DE (2) | DE1795581C3 (pt) |
| DK (3) | DK121122B (pt) |
| FR (5) | FR4011M (pt) |
| GB (3) | GB1101562A (pt) |
| IL (2) | IL22384A (pt) |
| MY (1) | MY7000168A (pt) |
| NL (3) | NL6412804A (pt) |
| NO (1) | NO133805C (pt) |
| SE (2) | SE318277B (pt) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3887551A (en) * | 1964-11-04 | 1975-06-03 | Glaxo Lab Ltd | Crystalline forms of cephaloridine |
| US3422099A (en) * | 1966-02-18 | 1969-01-14 | Bristol Myers Co | 7-(alpha-hydroxy-(2' or 3'-thienyl)-acetamido) cephalosporanic acids and related salts and derivatives |
| US3391141A (en) * | 1966-07-07 | 1968-07-02 | Bristol Myers Co | Synthetic cephalosporins |
| US3498979A (en) * | 1967-04-03 | 1970-03-03 | Glaxo Lab Ltd | Recovery of n-(7-2'-thienylacetamidoceph-3-em-3-ylmethyl) pyridinium - 4-carboxylate from an acid addition salt thereof |
| US3984403A (en) * | 1972-06-30 | 1976-10-05 | Takeda Chemical Industries, Ltd. | Arginine and lysine salts of acid cephalosporins |
| US4198504A (en) * | 1978-11-02 | 1980-04-15 | Bristol-Myers Company | [3-(Pyridinium)-7-(naphthyiridinyl carbonylamino)acetamido]cephalosporanic acid derivatives |
| NL8003003A (nl) * | 1979-05-25 | 1980-11-27 | Glaxo Group Ltd | Tussenprodukten te gebruiken bij de bereiding van cefalosporine antibiotica. |
| US4288590A (en) * | 1980-02-14 | 1981-09-08 | Bristol-Myers Company | 7-[Dα-(4-Hydroxy-1,5-naphthyridine-3-carboxamido)-α-arylacetamido]-3-(N,N-dimethyl-aminomethylpyridinium) methyl-3-cephem-4-carboxylates |
| DE3118732A1 (de) * | 1981-05-12 | 1982-12-02 | Hoechst Ag, 6000 Frankfurt | Cephalosporinderivate und verfahren zu ihrer herstellung |
| US4665168A (en) * | 1986-04-14 | 1987-05-12 | Eli Lilly And Company | Cephalosporin intermediate |
| US4734408A (en) * | 1986-12-17 | 1988-03-29 | Eli Lilly And Company | Crystalline cephalosporin antibiotic salts and solvates |
| KR940000112B1 (ko) * | 1990-07-05 | 1994-01-05 | 주식회사 대웅제약 | 신규의 3-치환 세펨화합물 및 그의 제조방법 |
| GB2270054A (en) * | 1992-08-29 | 1994-03-02 | Gen Motors France | Snap-fit steering column connection with lash adjuster. |
| SE0303570L (sv) * | 2003-12-03 | 2005-06-04 | Microdrug Ag | Fukt-känslig medicinsk produkt |
| AU2004294889B2 (en) * | 2003-12-03 | 2010-08-26 | Boehringer Ingelheim International Gmbh | Medical product containing tiotropium |
| US11582066B2 (en) | 2019-12-19 | 2023-02-14 | Cisco Technology, Inc. | Techniques for extending a cellular quality of service bearer through an enterprise fabric |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3218318A (en) * | 1962-08-31 | 1965-11-16 | Lilly Co Eli | 7-heterocyclic-substituted-acylamido cephalosporins |
| US3226384A (en) * | 1963-01-25 | 1965-12-28 | Nat Res Dev | Cephalosporin ca derivatives |
| US3225038A (en) * | 1963-06-05 | 1965-12-21 | Lilly Co Eli | Benzyl substituted-pyridinomethyl cephalosporins |
-
0
- GB GB1052068D patent/GB1052068A/en active Active
- FR FR116D patent/FR116F/fr active Active
-
1963
- 1963-11-04 GB GB39172/66A patent/GB1101562A/en not_active Expired
- 1963-11-04 GB GB43441/63A patent/GB1101561A/en not_active Expired
- 1963-12-13 FR FR957113A patent/FR4011M/fr not_active Expired
- 1963-12-13 FR FR957112A patent/FR1384197A/fr not_active Expired
- 1963-12-16 BE BE641338D patent/BE641338A/xx unknown
-
1964
- 1964-11-03 IL IL22384A patent/IL22384A/xx unknown
- 1964-11-03 IL IL26882A patent/IL26882A/xx unknown
- 1964-11-03 DK DK541264AA patent/DK121122B/da unknown
- 1964-11-04 NL NL6412804A patent/NL6412804A/xx unknown
- 1964-11-04 NO NO155414A patent/NO133805C/no unknown
- 1964-11-04 CH CH25768A patent/CH471078A/de not_active IP Right Cessation
- 1964-11-04 US US408757A patent/US3280118A/en not_active Expired - Lifetime
- 1964-11-04 DE DE1795581A patent/DE1795581C3/de not_active Expired
- 1964-11-04 FR FR993722A patent/FR1481034A/fr not_active Expired
- 1964-11-04 DE DE19641795609 patent/DE1795609A1/de active Pending
- 1964-11-04 CH CH1425264A patent/CH462171A/de unknown
- 1964-11-04 BE BE655273D patent/BE655273A/xx unknown
- 1964-11-04 SE SE13270/64A patent/SE318277B/xx unknown
- 1964-11-25 FR FR996254A patent/FR1414624A/fr not_active Expired
- 1964-11-27 US US414067A patent/US3313176A/en not_active Expired - Lifetime
-
1966
- 1966-08-19 JP JP41054274A patent/JPS5021530B1/ja active Pending
-
1967
- 1967-01-09 SE SE29167A patent/SE318278B/xx unknown
-
1969
- 1969-06-18 NL NL6909298A patent/NL6909298A/xx unknown
- 1969-11-14 DK DK603469AA patent/DK124758B/da unknown
-
1970
- 1970-08-18 CY CY55570A patent/CY555A/xx unknown
- 1970-09-23 NL NL707014054A patent/NL148060B/xx unknown
- 1970-12-31 MY MY1970168A patent/MY7000168A/xx unknown
-
1971
- 1971-02-12 DK DK63371AA patent/DK126205B/da unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL7014054A (en) | 1971-01-25 |
| FR4011M (pt) | 1966-03-21 |
| GB1052068A (pt) | |
| SE318278B (pt) | 1969-12-08 |
| NO133805C (pt) | 1976-06-30 |
| IL22384A (en) | 1968-04-25 |
| DE1445844A1 (de) | 1969-01-16 |
| FR1414624A (fr) | 1965-10-15 |
| FR1481034A (fr) | 1967-05-19 |
| NL6412804A (pt) | 1965-05-06 |
| DE1795581C3 (de) | 1978-09-07 |
| BE655273A (pt) | 1965-05-04 |
| US3280118A (en) | 1966-10-18 |
| JPS5021530B1 (pt) | 1975-07-23 |
| US3313176A (en) | 1967-04-11 |
| CH462171A (de) | 1968-09-15 |
| CY555A (en) | 1970-08-18 |
| FR1384197A (fr) | 1965-01-04 |
| FR116F (pt) | |
| DK124758B (da) | 1972-11-20 |
| DK126205B (da) | 1973-06-18 |
| SE318277B (pt) | 1969-12-08 |
| IL26882A (en) | 1968-04-25 |
| BE641338A (pt) | 1964-04-16 |
| CH471078A (de) | 1969-04-15 |
| DE1795609A1 (de) | 1972-04-27 |
| DK121122B (da) | 1971-09-13 |
| DE1795581B2 (de) | 1977-12-29 |
| NL148060B (nl) | 1975-12-15 |
| MY7000168A (en) | 1970-12-31 |
| NL6909298A (pt) | 1969-08-25 |
| DE1795610B2 (de) | 1975-08-28 |
| DE1795581A1 (de) | 1972-04-27 |
| GB1101561A (en) | 1968-01-31 |
| GB1101562A (en) | 1968-01-31 |
| DE1795610A1 (de) | 1972-04-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO133805B (pt) | ||
| SU577982A3 (ru) | Способ получени 2-тетрагидрофурфурил6,7-бензоморфанов или их солей | |
| CA2227264C (en) | Amine acid salt compounds and process for the production thereof | |
| US4394319A (en) | Co-ordination compound of platinum | |
| US6197998B1 (en) | Process for producing N-glycyltyrosine and its crystal structure | |
| NO155414B (no) | Anordning for mekanisk stamping av kald eller varm masse i en smelteinnretning, f.eks. smelteovn, digel e.l., samt anvendelse av slik anordning. | |
| EP0030871B1 (en) | Method of optical resolution of (+/-)-phenyl glycin and/or (+/-)-camphor sulfonic acid | |
| US3933902A (en) | Method for the optical resolution of DL-αphenylglycine | |
| US3532684A (en) | Molecular compounds of inosine and tryptophan | |
| US5049663A (en) | Process for producing 1-β-D-arabinofuranosylcytosine-5'-stearylphosphate monosodium salt and monohydrate thereof | |
| US4167633A (en) | Preparation of 2,4,5,6-tetraaminopyrimidine from 2,4,6-triaminopyrimidine | |
| KR100262684B1 (ko) | 폴린산의부분입체이성질체염의제조및분리방법 | |
| US3983109A (en) | Process for recovering cephalosporin C from A fermentation broth as the N-(p-nitrobenzoyl) derivative | |
| CN115611899B (zh) | 一种l-5-甲基四氢蝶酸的制备方法 | |
| US4845217A (en) | Purification of 5-pyrimidinecarboxamides | |
| CN116730906A (zh) | 酒石酸匹莫范色林晶型c制备方法 | |
| US4900826A (en) | Process for preparing N6,9-disubstituted adenine | |
| JP4275241B2 (ja) | Ｎ−グリシルチロシンの製造方法及びその結晶形 | |
| PL95335B1 (pl) | Sposob wytwarzania niehigroskopijnego chlorow rodiazepoksydu | |
| SU426469A1 (ru) | Способ получени ди-( -хлорэтил)аминопирилиевых солей | |
| KR0173084B1 (ko) | 트리아민 화합물의 정제방법 | |
| US5266704A (en) | Process for production of 2-substituted-4-hydromethylimidazole compounds | |
| US2891051A (en) | Adducts of salts of novobiocin | |
| JPH1087636A (ja) | 光学活性なＮ−ｔ−ブチル−２−ピペラジンアミドの製造方法 | |
| JPH01275595A (ja) | カナマイシン誘導体 |