FI105916B - Menetelmä terapeuttisesti käyttökelpoisten 3R-3,7-difenyyli-1,8-diatsaspiro[5,5]undekaanijohdannaisten valmistamiseksi - Google Patents
Menetelmä terapeuttisesti käyttökelpoisten 3R-3,7-difenyyli-1,8-diatsaspiro[5,5]undekaanijohdannaisten valmistamiseksi Download PDFInfo
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- FI105916B FI105916B FI941022A FI941022A FI105916B FI 105916 B FI105916 B FI 105916B FI 941022 A FI941022 A FI 941022A FI 941022 A FI941022 A FI 941022A FI 105916 B FI105916 B FI 105916B
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- phenyl
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- diazaspiro
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D211/74—Oxygen atoms
- C07D211/76—Oxygen atoms attached in position 2 or 6
Applications Claiming Priority (2)
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US2638293A | 1993-03-04 | 1993-03-04 | |
US2638293 | 1993-03-04 |
Publications (3)
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FI941022A0 FI941022A0 (fi) | 1994-03-03 |
FI941022A FI941022A (fi) | 1994-09-05 |
FI105916B true FI105916B (fi) | 2000-10-31 |
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FI941022A FI105916B (fi) | 1993-03-04 | 1994-03-03 | Menetelmä terapeuttisesti käyttökelpoisten 3R-3,7-difenyyli-1,8-diatsaspiro[5,5]undekaanijohdannaisten valmistamiseksi |
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US (1) | US5688806A (es) |
EP (1) | EP0687268B1 (es) |
JP (1) | JP2832754B2 (es) |
CN (1) | CN1099035A (es) |
AT (1) | ATE166650T1 (es) |
AU (1) | AU6226494A (es) |
CA (1) | CA2157117C (es) |
DE (1) | DE69318854T2 (es) |
DK (1) | DK0687268T3 (es) |
ES (1) | ES2116587T3 (es) |
FI (1) | FI105916B (es) |
IL (1) | IL108769A0 (es) |
WO (1) | WO1994020500A1 (es) |
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US5393762A (en) * | 1993-06-04 | 1995-02-28 | Pfizer Inc. | Pharmaceutical agents for treatment of emesis |
EP0655246A1 (en) * | 1993-11-30 | 1995-05-31 | Pfizer Inc. | Substance P antagonists for the treatment of disorders caused by helicobacter pylori or other spiral urease-positive gram-negative bacteria |
US5688960A (en) * | 1995-05-02 | 1997-11-18 | Schering Corporation | Substituted oximes, hydrazones and olefins useful as neurokinin antagonists |
US5696267A (en) * | 1995-05-02 | 1997-12-09 | Schering Corporation | Substituted oximes, hydrazones and olefins as neurokinin antagonists |
TW458774B (en) | 1995-10-20 | 2001-10-11 | Pfizer | Antiemetic pharmaceutical compositions |
EP1019410A1 (en) * | 1995-11-23 | 2000-07-19 | MERCK SHARP & DOHME LTD. | Spiro-piperidine derivatives and their use as tachykinin antagonists |
GB9603136D0 (en) * | 1996-02-15 | 1996-04-17 | Merck Sharp & Dohme | Therapeutic agents |
GB9603137D0 (en) * | 1996-02-15 | 1996-04-17 | Merck Sharp & Dohme | Therapeutic agents |
EP0888286B1 (en) * | 1996-03-14 | 2001-10-31 | Warner-Lambert Company | Novel substituted cyclic amino acids as pharmaceutical agents |
PL330235A1 (en) * | 1996-06-21 | 1999-05-10 | Merck Sharp & Dohme | Derivatives of spiropiperidine and their application as therapeutic agents |
GB9613969D0 (en) * | 1996-07-03 | 1996-09-04 | Merck Sharp & Dohme | Therapeutic agents |
US6046195A (en) * | 1996-09-25 | 2000-04-04 | Merck Sharp & Dohme Ltd. | Spiro-azacyclic derivatives, their preparation and their use as tachykinin antagonists |
US5929094A (en) * | 1996-10-25 | 1999-07-27 | Merck & Co., Inc. | Heteroaryl spiroethercycloalkyl tachykinin receptor antagonists |
GB9625843D0 (en) * | 1996-12-12 | 1997-01-29 | Merck & Co Inc | Phenyl spiroethercycloalkyl tachykinn receptor antagonists |
US5789422A (en) * | 1996-10-28 | 1998-08-04 | Schering Corporation | Substituted arylalkylamines as neurokinin antagonists |
US5945428A (en) * | 1996-11-01 | 1999-08-31 | Schering Corporation | Substituted oximes, hydrazones and olefins as neurokinin antagonists |
EP0942731B1 (en) * | 1996-12-02 | 2004-11-17 | MERCK SHARP & DOHME LTD. | Use of nk-1 receptor antagonists for treating substance use disorders |
GB9708484D0 (en) * | 1997-04-25 | 1997-06-18 | Merck Sharp & Dohme | Therapeutic agents |
GB9711114D0 (en) * | 1997-05-29 | 1997-07-23 | Merck Sharp & Dohme | Therapeutic agents |
US7101547B1 (en) | 1999-01-22 | 2006-09-05 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Method for the prevention and treatment of diseases caused by an inflammatory response mediated by endogenous substance P by using anti-substance P antibodies |
GB9902881D0 (en) * | 1999-02-09 | 1999-03-31 | Merck Sharp & Dohme | Therapeutic agents |
CA2324116A1 (en) * | 1999-10-25 | 2001-04-25 | Susan Beth Sobolov-Jaynes | Nk-1 receptor antagonists and eletriptan for the treatment of migraine |
EP1241257A4 (en) * | 1999-12-21 | 2005-03-16 | Takeda Pharmaceutical | TACHYKININ-SIMILAR POLYPEPTIDES AND ITS APPLICATION |
US20020049211A1 (en) * | 2000-09-06 | 2002-04-25 | Sobolov-Jaynes Susan Beth | Combination treatment for depression and anxiety |
EP1192952A3 (en) * | 2000-09-28 | 2003-03-26 | Pfizer Products Inc. | Combination, for treating depression and anxiety, containing an NK-3 receptor antagonist and a CNS penetrant NK-1 receptor antagonist |
JP2005504029A (ja) * | 2001-07-20 | 2005-02-10 | ファイザー・プロダクツ・インク | 犬の好ましくない行動を改善するためのnk−1受容体アンタゴニストの使用 |
KR101412339B1 (ko) | 2004-07-15 | 2014-06-25 | 알바니 몰레큘라 리써치, 인크. | 아릴- 및 헤테로아릴-치환된 테트라히드로이소퀴놀린, 및이것의 노르에피네프린, 도파민 및 세로토닌의 재흡수를차단하기 위한 용도 |
JP2008510711A (ja) * | 2004-08-20 | 2008-04-10 | ターガセプト,インコーポレイテッド | 嗜癖治療におけるn−アリールジアザスピラ環状化合物の使用 |
US8362075B2 (en) | 2005-05-17 | 2013-01-29 | Merck Sharp & Dohme Corp. | Cyclohexyl sulphones for treatment of cancer |
NZ565111A (en) | 2005-07-15 | 2011-10-28 | Amr Technology Inc | Aryl-and heteroaryl-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
WO2007041052A2 (en) | 2005-09-29 | 2007-04-12 | Merck & Co., Inc. | Acylated spiropiperidine derivatives as melanocortin-4 receptor modulators |
GB0603041D0 (en) | 2006-02-15 | 2006-03-29 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
WO2008039327A2 (en) | 2006-09-22 | 2008-04-03 | Merck & Co., Inc. | Method of treatment using fatty acid synthesis inhibitors |
US20110218176A1 (en) | 2006-11-01 | 2011-09-08 | Barbara Brooke Jennings-Spring | Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development |
WO2008084261A1 (en) | 2007-01-10 | 2008-07-17 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa | Amide substituted indazoles as poly(adp-ribose)polymerase (parp) inhibitors |
US8106086B2 (en) | 2007-04-02 | 2012-01-31 | Msd K.K. | Indoledione derivative |
EP2170076B1 (en) | 2007-06-27 | 2016-05-18 | Merck Sharp & Dohme Corp. | 4-carboxybenzylamino derivatives as histone deacetylase inhibitors |
CA2717509A1 (en) | 2008-03-03 | 2009-09-11 | Tiger Pharmatech | Tyrosine kinase inhibitors |
US9156812B2 (en) | 2008-06-04 | 2015-10-13 | Bristol-Myers Squibb Company | Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine |
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EP0273659A1 (en) * | 1986-12-27 | 1988-07-06 | Takeda Chemical Industries, Ltd. | Azaspiro compounds, their production and use |
ATE122353T1 (de) * | 1987-10-05 | 1995-05-15 | Yamanouchi Pharma Co Ltd | Heterozyklische spiroverbindungen und ihre herstellung. |
EP0360390A1 (en) * | 1988-07-25 | 1990-03-28 | Glaxo Group Limited | Spirolactam derivatives |
MX18467A (es) * | 1988-11-23 | 1993-07-01 | Pfizer | Agentes terapeuticos de quinuclidinas |
US5075317A (en) * | 1989-06-21 | 1991-12-24 | Fisons Corporation | Spirofurane derivatives |
DE69200921T2 (de) * | 1991-03-01 | 1995-05-04 | Pfizer | 1-azabicyclo[3.2.2]nonan-3-aminderivate. |
US5393762A (en) * | 1993-06-04 | 1995-02-28 | Pfizer Inc. | Pharmaceutical agents for treatment of emesis |
-
1993
- 1993-12-10 AU AU62264/94A patent/AU6226494A/en not_active Abandoned
- 1993-12-10 ES ES94909413T patent/ES2116587T3/es not_active Expired - Lifetime
- 1993-12-10 CA CA002157117A patent/CA2157117C/en not_active Expired - Fee Related
- 1993-12-10 EP EP94909413A patent/EP0687268B1/en not_active Expired - Lifetime
- 1993-12-10 AT AT94909413T patent/ATE166650T1/de not_active IP Right Cessation
- 1993-12-10 US US08/513,798 patent/US5688806A/en not_active Expired - Fee Related
- 1993-12-10 WO PCT/US1993/011793 patent/WO1994020500A1/en active IP Right Grant
- 1993-12-10 DK DK94909413T patent/DK0687268T3/da active
- 1993-12-10 DE DE69318854T patent/DE69318854T2/de not_active Expired - Fee Related
- 1993-12-10 JP JP6519951A patent/JP2832754B2/ja not_active Expired - Fee Related
-
1994
- 1994-02-24 IL IL10876994A patent/IL108769A0/xx unknown
- 1994-03-03 FI FI941022A patent/FI105916B/fi not_active IP Right Cessation
- 1994-03-03 CN CN94102227A patent/CN1099035A/zh active Pending
Also Published As
Publication number | Publication date |
---|---|
FI941022A0 (fi) | 1994-03-03 |
JPH08503226A (ja) | 1996-04-09 |
CN1099035A (zh) | 1995-02-22 |
JP2832754B2 (ja) | 1998-12-09 |
ATE166650T1 (de) | 1998-06-15 |
DE69318854D1 (de) | 1998-07-02 |
EP0687268B1 (en) | 1998-05-27 |
CA2157117C (en) | 1999-01-05 |
AU6226494A (en) | 1994-09-26 |
DK0687268T3 (da) | 1998-10-12 |
US5688806A (en) | 1997-11-18 |
ES2116587T3 (es) | 1998-07-16 |
WO1994020500A1 (en) | 1994-09-15 |
DE69318854T2 (de) | 1998-10-08 |
FI941022A (fi) | 1994-09-05 |
CA2157117A1 (en) | 1994-09-15 |
IL108769A0 (en) | 1994-06-24 |
EP0687268A1 (en) | 1995-12-20 |
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