KR860006441A - 피롤리딘 유도체의 제조방법 - Google Patents
피롤리딘 유도체의 제조방법 Download PDFInfo
- Publication number
- KR860006441A KR860006441A KR1019850000850A KR850000850A KR860006441A KR 860006441 A KR860006441 A KR 860006441A KR 1019850000850 A KR1019850000850 A KR 1019850000850A KR 850000850 A KR850000850 A KR 850000850A KR 860006441 A KR860006441 A KR 860006441A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- formula
- reaction
- iii
- carried out
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 11
- FKCMADOPPWWGNZ-YUMQZZPRSA-N [(2r)-1-[(2s)-2-amino-3-methylbutanoyl]pyrrolidin-2-yl]boronic acid Chemical compound CC(C)[C@H](N)C(=O)N1CCC[C@H]1B(O)O FKCMADOPPWWGNZ-YUMQZZPRSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 10
- 238000006243 chemical reaction Methods 0.000 claims 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 238000006698 hydrazinolysis reaction Methods 0.000 claims 2
- 230000007062 hydrolysis Effects 0.000 claims 2
- 238000006460 hydrolysis reaction Methods 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims 2
- 235000011181 potassium carbonates Nutrition 0.000 claims 2
- 235000011118 potassium hydroxide Nutrition 0.000 claims 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims 2
- 235000017550 sodium carbonate Nutrition 0.000 claims 2
- 235000011121 sodium hydroxide Nutrition 0.000 claims 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 2
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 claims 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 235000011114 ammonium hydroxide Nutrition 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 1
- -1 hydrazine anhydride Chemical class 0.000 claims 1
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Chemical group 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 239000011736 potassium bicarbonate Substances 0.000 claims 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims 1
- 235000015497 potassium bicarbonate Nutrition 0.000 claims 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 230000035484 reaction time Effects 0.000 claims 1
- 239000001632 sodium acetate Substances 0.000 claims 1
- 235000017281 sodium acetate Nutrition 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Heart & Thoracic Surgery (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pyrrole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Description
Claims (11)
- 다음 구조식 (Ⅲ) 화합물을 다음 구조식 (Ⅳ) 화합물과 반응시켜 얻은 다음 구조식 (Ⅱ) 화합물을 가수분해 혹은 히드라지놀리시스시키거나 에틸렌디아민과 반응시킴을 특징으로 하는 다음 구조식 (Ⅰ) 화합물의 제조방법.상기 구조식에서 X는 염소 혹은 브롬이며, Y는 산소 혹은 질소 원자이고, R은 탄소수 1 내지 5의 저급 알킬이고, n은 1 또는 2의 정수이고(단, Y가 질소일 때는 2이고, Y가 산소일 때는 1임), M은 나트룸 혹은 칼륨원자이다.
- 제 1 항에 있어서, 상기 구조식 (Ⅲ)과 (Ⅳ) 화합물을 반응시킴에 있어, 용매로서 물 혹은 메탄올, 에탄올, 아세톤, 1,4-디옥산, 테트라하이드로푸란, N,N-디메틸포름아미드, 디메틸술폭사이드 혹은 이들 용매의 수용액을 사용함을 특징으로 하는 방법.
- 제 2 항에 있어서, 화합물 (Ⅳ)을 화합물 (Ⅲ)에 대해 1 내지 3배 몰비로 사용함을 특징으로 하는 방법.
- 제 2 항에 있어서, 반응온도 및 반응시간을 35℃ 내지 120℃ 및 30분 내지 20시간으로 하여 수행함을 특징으로 하는 방법.
- 제 2 항에 있어서, 염기로서 중탄산나트륨, 탄산나트륨, 수산화나트륨, 중탄산칼륨, 탄산칼륨, 수산화칼륨, 나트륨아세데이트, 피리딘 또는 트리에틸아민을 구조식 (Ⅲ) 화합물에 대해 0.5 내지 2.5배 몰비로 사용하며 반응시킴을 특징으로 하는 방법.
- 제 1 항에 있어서, 상기 구조식 (Ⅱ) 화합물의 가수분해는 수산화칼륨, 탄산칼륨, 수산화나트륨, 탄산나트륨 혹은 암모니아수를 사용하여 수행함을 특징으로 하는 방법.
- 제 1 항에 있어서, 상기 구조식 (Ⅱ) 화합물의 히드라지놀리시스 반응은 히드라진 무수물 혹은 히드라진 수화물을 상기 구조식 (Ⅱ) 화합물에 대해 1 내지 5배 몰비로 사용하여 수행함을 특징으로 하는 방법.
- 제 7 항에 있어서, 반응온도를 40℃ 내지 130℃로 하여 수행함을 특징으로 하는 방법.
- 제 1 항에 있어서, 상기 구조식 (Ⅱ) 화합물을 에틸렌디아민과 반응시킴에 있어 구조식 (Ⅲ) 화합물에 대해 에틸렌디아민의 양을 1 내지 10배 몰비로 하여 수행함을 특징으로 하는 방법.
- 제 9 항에 있어서, 반응을 10℃ 내지 80℃에서 수행함을 특징으로 하는 방법.
- 제 9 항에 있어서, 반응을 카본테트라 클로라이드, 클로로포롬, 메틸렌클로라이드, 에틸아세테이트, 테트라하이드로푸란, 1,4-디옥산 혹은 알콜류와 같은 용매 존재 또는 부재하에 수행함을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019850000850A KR870001569B1 (ko) | 1985-02-11 | 1985-02-11 | 피롤리딘 유도체의 제조방법 |
DE19853538747 DE3538747A1 (de) | 1985-02-11 | 1985-10-31 | Verfahren zur herstellung von pyrrolidin-derivaten |
ES548744A ES8606269A1 (es) | 1985-02-11 | 1985-11-11 | Procedimiento para preparar un derivado de pirrolidina |
JP60282703A JPS61183263A (ja) | 1985-02-11 | 1985-12-16 | ピロリジン誘導体の製造方法 |
GB08602782A GB2170806B (en) | 1985-02-11 | 1986-02-05 | 1-(3 mercapto-2-methylpropionyl)-l-proline, precursors thereof and processes for their preparation |
FR8601839A FR2577222B1 (fr) | 1985-02-11 | 1986-02-11 | Procede pour la preparation de l'acide 1-(3-mercapto-25-methylpropionyl)-pyrrolidine-(25)-carboxylique |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019850000850A KR870001569B1 (ko) | 1985-02-11 | 1985-02-11 | 피롤리딘 유도체의 제조방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR860006441A true KR860006441A (ko) | 1986-09-11 |
KR870001569B1 KR870001569B1 (ko) | 1987-09-04 |
Family
ID=19239706
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019850000850A KR870001569B1 (ko) | 1985-02-11 | 1985-02-11 | 피롤리딘 유도체의 제조방법 |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS61183263A (ko) |
KR (1) | KR870001569B1 (ko) |
DE (1) | DE3538747A1 (ko) |
ES (1) | ES8606269A1 (ko) |
FR (1) | FR2577222B1 (ko) |
GB (1) | GB2170806B (ko) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HU208954B (en) * | 1990-09-21 | 1994-02-28 | Egyt Gyogyszervegyeszeti Gyar | Process for producing 1-(3-mercapto-(2s)-methyl-1-oxo-propyl)-l-prolyn |
US5237073A (en) * | 1988-08-26 | 1993-08-17 | Sepracor, Inc. | Derivatives and precursors of captopril and its analogues |
WO1990002118A1 (en) * | 1988-08-26 | 1990-03-08 | Sepracor, Inc. | Derivatives and precursors of captopril and its analogues |
KR940005014B1 (ko) * | 1991-11-07 | 1994-06-09 | 보령제약 주식회사 | 피롤리딘카르복실산 유도체의 제조방법 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU509899B2 (en) * | 1976-02-13 | 1980-05-29 | E.R. Squibb & Sons, Inc. | Proline derivatives and related compounds |
US4046889A (en) * | 1976-02-13 | 1977-09-06 | E. R. Squibb & Sons, Inc. | Azetidine-2-carboxylic acid derivatives |
US4192945A (en) * | 1978-12-07 | 1980-03-11 | E. R. Squibb & Sons, Inc. | Process for preparing proline and homoproline derivatives |
GB2065643B (en) * | 1979-12-13 | 1983-08-24 | Kanegafuchi Chemical Ind | Optically active n-mercaptoalkanoylamino acids |
HU184082B (en) * | 1979-12-29 | 1984-06-28 | Egyt Gyogyszervegyeszeti Gyar | Process for preparing 1-3-/3mercapto-/2s/-methyl-propinyl/-pyrrolidine-/2s/-carboxylic acid |
JPS58124764A (ja) * | 1982-01-20 | 1983-07-25 | Kanegafuchi Chem Ind Co Ltd | 光学活性チオ−ル化合物の製造法 |
-
1985
- 1985-02-11 KR KR1019850000850A patent/KR870001569B1/ko not_active IP Right Cessation
- 1985-10-31 DE DE19853538747 patent/DE3538747A1/de active Granted
- 1985-11-11 ES ES548744A patent/ES8606269A1/es not_active Expired
- 1985-12-16 JP JP60282703A patent/JPS61183263A/ja active Pending
-
1986
- 1986-02-05 GB GB08602782A patent/GB2170806B/en not_active Expired
- 1986-02-11 FR FR8601839A patent/FR2577222B1/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB8602782D0 (en) | 1986-03-12 |
GB2170806A (en) | 1986-08-13 |
DE3538747C2 (ko) | 1988-08-18 |
JPS61183263A (ja) | 1986-08-15 |
ES8606269A1 (es) | 1986-04-01 |
FR2577222B1 (fr) | 1987-12-24 |
FR2577222A1 (fr) | 1986-08-14 |
DE3538747A1 (de) | 1986-08-14 |
GB2170806B (en) | 1988-08-03 |
ES548744A0 (es) | 1986-04-01 |
KR870001569B1 (ko) | 1987-09-04 |
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