NZ243255A - 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-4-spiro-3'-pyrrolidine-1,2',3 ,5'-tetrone derivatives; medicaments and preparation - Google Patents
1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-4-spiro-3'-pyrrolidine-1,2',3 ,5'-tetrone derivatives; medicaments and preparationInfo
- Publication number
- NZ243255A NZ243255A NZ243255A NZ24325592A NZ243255A NZ 243255 A NZ243255 A NZ 243255A NZ 243255 A NZ243255 A NZ 243255A NZ 24325592 A NZ24325592 A NZ 24325592A NZ 243255 A NZ243255 A NZ 243255A
- Authority
- NZ
- New Zealand
- Prior art keywords
- compound
- pyrazine
- tetrahydropyrrolo
- hydrogen
- spiro
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title abstract description 52
- 239000003814 drug Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 243
- 238000000034 method Methods 0.000 claims abstract description 35
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 28
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 27
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 27
- 150000002367 halogens Chemical class 0.000 claims abstract description 27
- 239000001257 hydrogen Substances 0.000 claims abstract description 27
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 27
- 150000003839 salts Chemical class 0.000 claims abstract description 22
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 20
- 102000016912 Aldehyde Reductase Human genes 0.000 claims abstract description 19
- 108010053754 Aldehyde reductase Proteins 0.000 claims abstract description 19
- 230000008569 process Effects 0.000 claims abstract description 18
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 13
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 189
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 45
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 26
- 239000000126 substance Substances 0.000 claims description 12
- 150000002431 hydrogen Chemical class 0.000 claims description 11
- 230000003389 potentiating effect Effects 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 238000007796 conventional method Methods 0.000 claims description 6
- 150000001721 carbon Chemical group 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 4
- 239000008187 granular material Substances 0.000 claims description 4
- GXWNSJYVSIJRLS-UHFFFAOYSA-N 6-bromo-8-methylimidazo[1,2-a]pyrazine Chemical group CC1=NC(Br)=CN2C=CN=C12 GXWNSJYVSIJRLS-UHFFFAOYSA-N 0.000 claims description 3
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 230000002140 halogenating effect Effects 0.000 claims description 3
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 3
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 3
- 235000012239 silicon dioxide Nutrition 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000003554 tetrahydropyrrolyl group Chemical group 0.000 claims 1
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- 206010012655 Diabetic complications Diseases 0.000 abstract description 10
- 238000011282 treatment Methods 0.000 abstract description 9
- 230000002265 prevention Effects 0.000 abstract description 8
- USIPCBPGIIPILV-UHFFFAOYSA-N spiro[2,3-dihydro-1h-pyrrolo[1,2-a]pyrazine-4,3'-pyrrolidine] Chemical class C1NCCC21N1C=CC=C1CNC2 USIPCBPGIIPILV-UHFFFAOYSA-N 0.000 abstract description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 80
- 230000002829 reductive effect Effects 0.000 description 65
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 60
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 58
- 239000000243 solution Substances 0.000 description 55
- 238000006243 chemical reaction Methods 0.000 description 53
- 239000000203 mixture Substances 0.000 description 48
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 42
- -1 methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, pentyloxy Chemical group 0.000 description 37
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 33
- 239000013078 crystal Substances 0.000 description 31
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- 239000003480 eluent Substances 0.000 description 20
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- RKOTXQYWCBGZLP-UHFFFAOYSA-N N-[(2,4-difluorophenyl)methyl]-2-ethyl-9-hydroxy-3-methoxy-1,8-dioxospiro[3H-pyrido[1,2-a]pyrazine-4,3'-oxolane]-7-carboxamide Chemical compound CCN1C(OC)C2(CCOC2)N2C=C(C(=O)NCC3=C(F)C=C(F)C=C3)C(=O)C(O)=C2C1=O RKOTXQYWCBGZLP-UHFFFAOYSA-N 0.000 description 9
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- 206010012601 diabetes mellitus Diseases 0.000 description 9
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- 102000004190 Enzymes Human genes 0.000 description 8
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- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 7
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/20—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP03183185 | 1991-06-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ243255A true NZ243255A (en) | 1994-03-25 |
Family
ID=16131263
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ243255A NZ243255A (en) | 1991-06-26 | 1992-06-22 | 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-4-spiro-3'-pyrrolidine-1,2',3 ,5'-tetrone derivatives; medicaments and preparation |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US5258382A (enEXAMPLES) |
| EP (1) | EP0520320B1 (enEXAMPLES) |
| JP (1) | JP2516147B2 (enEXAMPLES) |
| KR (1) | KR100241196B1 (enEXAMPLES) |
| CN (1) | CN1034176C (enEXAMPLES) |
| AT (1) | ATE157980T1 (enEXAMPLES) |
| AU (1) | AU648901B2 (enEXAMPLES) |
| CA (1) | CA2071273C (enEXAMPLES) |
| DE (1) | DE69222096T2 (enEXAMPLES) |
| DK (1) | DK0520320T3 (enEXAMPLES) |
| ES (1) | ES2108717T3 (enEXAMPLES) |
| FI (1) | FI98066C (enEXAMPLES) |
| GR (1) | GR3024870T3 (enEXAMPLES) |
| HK (1) | HK1001728A1 (enEXAMPLES) |
| HU (1) | HU218214B (enEXAMPLES) |
| IE (1) | IE921891A1 (enEXAMPLES) |
| MX (1) | MX9203231A (enEXAMPLES) |
| NO (1) | NO300637B1 (enEXAMPLES) |
| NZ (1) | NZ243255A (enEXAMPLES) |
| TW (1) | TW202450B (enEXAMPLES) |
| ZA (1) | ZA924425B (enEXAMPLES) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3195455B2 (ja) * | 1993-01-06 | 2001-08-06 | ウェルファイド株式会社 | キノリン−３−酢酸誘導体、その製造法と用途 |
| JP3681082B2 (ja) * | 1996-06-27 | 2005-08-10 | 住友ベークライト株式会社 | イミド環含有エポキシ樹脂及びエポキシ樹脂組成物 |
| KR100571613B1 (ko) * | 1997-10-20 | 2006-04-17 | 다이닛본 스미토모 세이야꾸 가부시끼가이샤 | 안정화 의약 조성물 |
| BR9814090A (pt) * | 1997-10-20 | 2000-10-03 | Dainippon Pharmaceutical Co | Composição de drogas rapidamente solúvel |
| JP2007246539A (ja) * | 1997-10-20 | 2007-09-27 | Dainippon Sumitomo Pharma Co Ltd | 速溶性医薬組成物 |
| TWI271192B (en) * | 1999-11-11 | 2007-01-21 | Kyorin Pharmaceutical Co Ltd | Solid formulation for oral administration |
| MXPA02006134A (es) | 1999-12-21 | 2002-12-13 | Guilford Pharm Inc | Compuestos derivados de hidantoina, composiciones farmaceuticas y metodos de uso de los mismos. |
| US20060058310A1 (en) * | 2002-11-14 | 2006-03-16 | Yoshifumi Takenobu | Remedies for vertebral canal stenosis |
| CA2656921A1 (en) | 2006-07-07 | 2008-01-10 | Dainippon Sumitomo Pharma Co., Ltd. | 3-hydrazino-2,5-dioxopyrrolidine-3-carboxylates and a process for preparing the same as well as a use of the same |
| WO2008026678A1 (fr) * | 2006-08-31 | 2008-03-06 | Dainippon Sumitomo Pharma Co., Ltd. | Derive de diester d'acide succinique, procede de production associe et utilisation de ce derive dans la production d'une preparation pharmaceutique |
| JP5149802B2 (ja) * | 2006-09-20 | 2013-02-20 | 日産化学工業株式会社 | 光学活性コハク酸イミド化合物の製造法 |
| KR20090057388A (ko) * | 2006-09-27 | 2009-06-05 | 닛산 가가쿠 고교 가부시키 가이샤 | 숙신이미드 화합물의 제조 방법 |
| US20110190497A1 (en) * | 2006-09-29 | 2011-08-04 | Daisuke Tanaka | Process for production of 2,5 dioxopyrrolidine 3 carboxylate |
| EP2095812A4 (en) | 2006-10-25 | 2011-07-13 | Dainippon Sumitomo Pharma Co | NON-AGGLUTINANT GRANULAR PREPARATION |
| WO2008081860A1 (ja) * | 2006-12-28 | 2008-07-10 | Dainippon Sumitomo Pharma Co., Ltd. | 光学活性コハク酸イミド誘導体およびその製造方法ならびにその使用 |
| JPWO2008136527A1 (ja) * | 2007-05-08 | 2010-07-29 | 大日本住友製薬株式会社 | 光学活性ジオキソピロリジン誘導体の精製方法 |
| EP2164488A1 (en) * | 2007-07-13 | 2010-03-24 | Eisai R&D Management Co., Ltd. | Ampa receptor antagonists and aldose reductase inhibitors for neuropathic pain |
| JP2011026201A (ja) * | 2007-10-17 | 2011-02-10 | Mitsubishi Tanabe Pharma Corp | 光学活性ピロリル−コハク酸イミド誘導体の立体選択的な製造方法 |
| WO2010090031A1 (ja) | 2009-02-06 | 2010-08-12 | 大日本住友製薬株式会社 | 光学活性スクシンイミド誘導体の製造方法及びその中間体 |
| WO2012014953A1 (ja) | 2010-07-29 | 2012-02-02 | 大日本住友製薬株式会社 | 光学活性スクシンイミド誘導体の製造方法 |
| EP2671589A4 (en) | 2011-02-02 | 2014-11-19 | Public Univ Corp Nagoya City Univ | MEDICAMENT FOR PREVENTING OR TREATING DISEASES RELATED TO INTRAOCULAR NEOVASCULARIZATION AND / OR INTRAOCULAR VASCULAR HYPERPERMEABILITY |
| US10034880B2 (en) * | 2014-09-11 | 2018-07-31 | Sumitomo Dainippon Pharma Co., Ltd. | Ophthalmic suspension formulation |
| CN106928234A (zh) * | 2017-02-07 | 2017-07-07 | 上海合全药业股份有限公司 | （2‑苄基‑1,2,3,4‑四氢吡咯并[1,2‑a]吡嗪）‑4‑甲醇的合成方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60142984A (ja) * | 1983-12-28 | 1985-07-29 | Kyorin Pharmaceut Co Ltd | 新規なスピロピロリジン−２，５−ジオン誘導体およびその製造法 |
| US4656169A (en) * | 1984-08-14 | 1987-04-07 | Pfizer Inc. | Tetracyclic spiro-hydantoin aldose reductase inhibitors and compositions |
| JPS63132889A (ja) * | 1986-11-21 | 1988-06-04 | Tanabe Seiyaku Co Ltd | キナゾリノン誘導体 |
| AU617541B2 (en) * | 1988-10-20 | 1991-11-28 | Wyeth | Spiro-isoquinoline-pyrrolidine tetrones and analogs thereof useful as aldose reductase inhibitors |
-
1992
- 1992-06-13 TW TW081104635A patent/TW202450B/zh active
- 1992-06-15 CA CA002071273A patent/CA2071273C/en not_active Expired - Lifetime
- 1992-06-17 DE DE69222096T patent/DE69222096T2/de not_active Expired - Lifetime
- 1992-06-17 AT AT92110270T patent/ATE157980T1/de active
- 1992-06-17 DK DK92110270.3T patent/DK0520320T3/da active
- 1992-06-17 ZA ZA924425A patent/ZA924425B/xx unknown
- 1992-06-17 EP EP92110270A patent/EP0520320B1/en not_active Expired - Lifetime
- 1992-06-17 ES ES92110270T patent/ES2108717T3/es not_active Expired - Lifetime
- 1992-06-18 FI FI922848A patent/FI98066C/fi not_active IP Right Cessation
- 1992-06-19 KR KR1019920010679A patent/KR100241196B1/ko not_active Expired - Lifetime
- 1992-06-19 US US07/901,029 patent/US5258382A/en not_active Expired - Lifetime
- 1992-06-22 NZ NZ243255A patent/NZ243255A/en not_active IP Right Cessation
- 1992-06-24 MX MX9203231A patent/MX9203231A/es unknown
- 1992-06-24 AU AU18483/92A patent/AU648901B2/en not_active Expired
- 1992-06-24 HU HU9202105A patent/HU218214B/hu unknown
- 1992-06-25 NO NO922512A patent/NO300637B1/no not_active IP Right Cessation
- 1992-06-25 JP JP4193074A patent/JP2516147B2/ja not_active Expired - Lifetime
- 1992-06-26 CN CN92108832A patent/CN1034176C/zh not_active Expired - Lifetime
- 1992-07-01 IE IE189192A patent/IE921891A1/en not_active IP Right Cessation
-
1997
- 1997-09-26 GR GR970402515T patent/GR3024870T3/el unknown
-
1998
- 1998-01-23 HK HK98100610A patent/HK1001728A1/en not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RENW | Renewal (renewal fees accepted) | ||
| RENW | Renewal (renewal fees accepted) | ||
| ASS | Change of ownership |
Owner name: DAINIPPON SUMITOMO PHARMA CO., JP Free format text: OLD OWNER(S): DAINIPPON PHARMACEUTICAL CO., LTD. |
|
| EXPY | Patent expired |