JP2002520316A5 - - Google Patents
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- Publication number
- JP2002520316A5 JP2002520316A5 JP2000559090A JP2000559090A JP2002520316A5 JP 2002520316 A5 JP2002520316 A5 JP 2002520316A5 JP 2000559090 A JP2000559090 A JP 2000559090A JP 2000559090 A JP2000559090 A JP 2000559090A JP 2002520316 A5 JP2002520316 A5 JP 2002520316A5
- Authority
- JP
- Japan
- Prior art keywords
- hydrogen
- compound
- alkyl
- alkylcarbamoyl
- alkoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 description 17
- 229910052739 hydrogen Inorganic materials 0.000 description 12
- 239000001257 hydrogen Substances 0.000 description 12
- -1 2-oxo-tetrahydro-1 (2H) -pyrimidinyl Chemical group 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 125000003545 alkoxy group Chemical group 0.000 description 8
- 125000005115 alkyl carbamoyl group Chemical group 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 125000001475 halogen functional group Chemical group 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 125000005236 alkanoylamino group Chemical group 0.000 description 3
- 125000005281 alkyl ureido group Chemical group 0.000 description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 3
- 125000004093 cyano group Chemical group *C#N 0.000 description 3
- 238000001727 in vivo Methods 0.000 description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 description 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 description 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 2
- 125000001589 carboacyl group Chemical group 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 125000006624 (C1-C6) alkoxycarbonylamino group Chemical group 0.000 description 1
- SJHZTGDJTIZMSK-KPRDSAADSA-N 3-cyano-n-[(2s)-2-(3,4-dichlorophenyl)-4-[4-[2-[(s)-methylsulfinyl]phenyl]piperidin-1-yl]butyl]-n-methylnaphthalene-1-carboxamide Chemical compound C([C@H](CN(C)C(=O)C=1C2=CC=CC=C2C=C(C=1)C#N)C=1C=C(Cl)C(Cl)=CC=1)CN(CC1)CCC1C1=CC=CC=C1[S@](C)=O SJHZTGDJTIZMSK-KPRDSAADSA-N 0.000 description 1
- VHQVJYKYAGBACO-UDKJZQBVSA-N 3-cyano-n-[(2s)-2-(3,4-dichlorophenyl)-4-[4-[4-methoxy-2-[(s)-methylsulfinyl]phenyl]piperidin-1-yl]butyl]-n-methylnaphthalene-1-carboxamide Chemical compound C[S@](=O)C1=CC(OC)=CC=C1C1CCN(CC[C@H](CN(C)C(=O)C=2C3=CC=CC=C3C=C(C=2)C#N)C=2C=C(Cl)C(Cl)=CC=2)CC1 VHQVJYKYAGBACO-UDKJZQBVSA-N 0.000 description 1
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 description 1
- 0 Cc1c(C(N(C)C[C@@](CCN(CC2)CCC2c2ccc(*)cc2[S@@](C)=O)c(cc2)cc(Cl)c2Cl)=O)c(ccc(*)c2)c2c(*)c1* Chemical compound Cc1c(C(N(C)C[C@@](CCN(CC2)CCC2c2ccc(*)cc2[S@@](C)=O)c(cc2)cc(Cl)c2Cl)=O)c(ccc(*)c2)c2c(*)c1* 0.000 description 1
- 125000005118 N-alkylcarbamoyl group Chemical group 0.000 description 1
- 102000007124 Tachykinin Receptors Human genes 0.000 description 1
- 108010072901 Tachykinin Receptors Proteins 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000003441 thioacyl group Chemical group 0.000 description 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9814886.9A GB9814886D0 (en) | 1998-07-10 | 1998-07-10 | N-Substituted naphthalenecarboxamides |
| GB9814886.9 | 1998-07-10 | ||
| GBGB9821703.7A GB9821703D0 (en) | 1998-10-07 | 1998-10-07 | Compounds |
| GB9821699.7 | 1998-10-07 | ||
| GBGB9821699.7A GB9821699D0 (en) | 1998-10-07 | 1998-10-07 | Compounds |
| GB9821703.7 | 1998-10-07 | ||
| GB9909840.2 | 1999-04-30 | ||
| GBGB9909840.2A GB9909840D0 (en) | 1999-04-30 | 1999-04-30 | Compounds |
| PCT/GB1999/002178 WO2000002859A1 (en) | 1998-07-10 | 1999-07-07 | N-substituted naphthalene carboxamides as neurokinin-receptor antagonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002520316A JP2002520316A (ja) | 2002-07-09 |
| JP2002520316A5 true JP2002520316A5 (https=) | 2006-08-03 |
Family
ID=27451806
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000559090A Pending JP2002520316A (ja) | 1998-07-10 | 1999-07-07 | ニューロキニン受容体アンタゴニストとしてのｎ−置換ナフタレンカルボキサミド |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6365602B1 (https=) |
| EP (1) | EP1097137A1 (https=) |
| JP (1) | JP2002520316A (https=) |
| KR (1) | KR20010083100A (https=) |
| CN (1) | CN1309638A (https=) |
| AR (1) | AR019365A1 (https=) |
| AU (1) | AU4637899A (https=) |
| BR (1) | BR9912013A (https=) |
| CA (1) | CA2336806A1 (https=) |
| ID (1) | ID24739A (https=) |
| IL (1) | IL140770A0 (https=) |
| NO (1) | NO20010151L (https=) |
| WO (1) | WO2000002859A1 (https=) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001014336A1 (en) * | 1999-08-20 | 2001-03-01 | Nippon Kayaku Kabushiki Kaisha | Benzene derivatives substituted by aromatic ring and process for producing the same |
| US6271418B1 (en) | 2000-02-22 | 2001-08-07 | Nippon Kayaku Co., Ltd. | Process for preparing (hetero) aromatic substituted benzene derivatives |
| US6903092B2 (en) | 2000-04-06 | 2005-06-07 | Peter Bernstein | Naphthamide neurokinin antagonists for use as medicaments |
| EP1276729B1 (en) * | 2000-04-06 | 2008-07-09 | AstraZeneca AB | New neurokinin antagonists for use as medicaments |
| US6846814B2 (en) | 2000-04-06 | 2005-01-25 | Astra Zeneca Ab | Neurokinin antagonists for use as medicaments |
| DE60114597T2 (de) * | 2000-04-06 | 2006-07-20 | Astrazeneca Ab | Naphthamid-neurokinin antagonisten zur verwendung als medikamente |
| GB0015246D0 (en) * | 2000-06-22 | 2000-08-16 | Astrazeneca Ab | Method for the treatment of urinary incontinence |
| FR2813891B1 (fr) * | 2000-09-14 | 2005-01-14 | Immunotech Sa | Reactif multifonctionnel pour erythrocytes mettant en jeu des carbamates et applications |
| EP1322309B1 (en) * | 2000-09-29 | 2008-08-13 | Neurogen Corporation | High affinity small molecule c5a receptor modulators |
| SE0004827D0 (sv) * | 2000-12-22 | 2000-12-22 | Astrazeneca Ab | Therapeutic compounds |
| US6727264B1 (en) * | 2001-07-05 | 2004-04-27 | Synaptic Pharmaceutical Corporation | Substituted anilinic piperidines as MCH selective antagonists |
| WO2003043987A2 (en) * | 2001-11-19 | 2003-05-30 | Elan Pharmaceuticals, Inc. | (4-phenyl) piperidin-3-yl-phenylcarboxylate derivatives and related compounds as beta-secretase inhibitors for the treatment of alzheimer's disease |
| WO2004020411A1 (en) * | 2002-08-29 | 2004-03-11 | Astrazeneca Ab | Naphthamide derivatives and their use |
| EP1560769B1 (en) * | 2002-11-05 | 2008-02-27 | AstraZeneca AB | Locking arrangement for a closure on a container and corresponding container |
| ES2286470T3 (es) * | 2002-12-20 | 2007-12-01 | Astrazeneca Ab | Compuestos de 4-aril-4-(naft-1-ilmetilamino)metil-piperidina y su uso. |
| TW200508221A (en) | 2003-06-13 | 2005-03-01 | Astrazeneca Ab | New azetidine compounds |
| TW200524868A (en) * | 2003-07-31 | 2005-08-01 | Zeria Pharm Co Ltd | Benzylamine derivatives |
| SE0403005D0 (sv) * | 2004-12-09 | 2004-12-09 | Astrazeneca Ab | New use |
| JP2008546768A (ja) * | 2005-06-23 | 2008-12-25 | アストラゼネカ・アクチエボラーグ | 胃腸疾患を治療するためのニューロキニン受容体アンタゴニストとしての新規なアゼチジン誘導体 |
| KR20080036957A (ko) * | 2005-06-23 | 2008-04-29 | 아스트라제네카 아베 | 위장 질환 치료용 뉴로키닌 수용체 길항제로서의 신규한아제티딘 유도체 |
| AR056087A1 (es) * | 2005-09-29 | 2007-09-19 | Astrazeneca Ab | Derivados de azetidina como antagonistas de receptores de neuroquina nk |
| AR057828A1 (es) | 2005-09-29 | 2007-12-19 | Astrazeneca Ab | Compuestos derivados de azetidina, su preparacion y composicion farmaceuutica |
| US20070219214A1 (en) * | 2006-02-01 | 2007-09-20 | Solvay Pharmaceuticals Gmbh | Dual NK2/NK3-antagonists, pharmaceutical compositions comprising them, and processes for their preparation |
| EP1979319A1 (en) * | 2006-02-01 | 2008-10-15 | Solvay Pharmaceuticals GmbH | Novel dual nk2/nk3-antagonists, pharmaceutical compositions comprising them and processes for their preparations |
| US8106208B2 (en) | 2006-05-18 | 2012-01-31 | Albireo Ab | Benzamide compounds that act as NK receptor antagonists |
| WO2008090114A1 (en) | 2007-01-24 | 2008-07-31 | Glaxo Group Limited | Pharmaceutical compositions comprising 2-methoxy-5- (5-trifluoromethyl-tetrazol-i-yl-benzyl) - (2s-phenyl-piperidin-3s-yl-) |
| US8304433B2 (en) * | 2008-11-14 | 2012-11-06 | Theravance, Inc. | Crystalline form of a 4-[2-(2-fluorophenoxymethyl)phenyl]piperidine compound |
| CN116754685B (zh) * | 2023-07-07 | 2025-07-25 | 浙江新和成特种材料有限公司 | 一种利用高效液相色谱法测定pps浆料母液中甲硫醇钠含量的方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IE903957A1 (en) * | 1989-11-06 | 1991-05-08 | Sanofi Sa | Aromatic amine compounds, their method of preparation and¹pharmaceutical compositions in which they are present |
| IL99320A (en) | 1990-09-05 | 1995-07-31 | Sanofi Sa | Arylalkylamines, their preparation and pharmaceutical compositions containing them |
| JP2999829B2 (ja) * | 1990-12-31 | 2000-01-17 | 株式会社資生堂 | 皮膚外用剤 |
| FR2676054B1 (fr) | 1991-05-03 | 1993-09-03 | Sanofi Elf | Nouveaux composes n-alkylenepiperidino et leurs enantiomeres, procede pour leur preparation et compositions pharmaceutiques les contenant. |
| FR2688219B1 (fr) | 1992-03-03 | 1994-07-08 | Sanofi Elf | Sels d'ammonium quaternaires de composes aromatiques amines, leur preparation et compositions pharmaceutiques les contenant. |
| GB9310713D0 (en) | 1993-05-24 | 1993-07-07 | Zeneca Ltd | Aryl substituted heterocycles |
| JPH06340526A (ja) * | 1993-06-02 | 1994-12-13 | Mitsui Toatsu Chem Inc | 置換１，４−ナフトキノン誘導体を有効成分として含有する神経成長因子産生、分泌誘発剤 |
| GB9617730D0 (en) * | 1996-08-23 | 1996-10-02 | Pfizer Ltd | Quarternary ammonium compounds |
-
1999
- 1999-07-07 CN CN99808501A patent/CN1309638A/zh active Pending
- 1999-07-07 EP EP99929597A patent/EP1097137A1/en not_active Withdrawn
- 1999-07-07 AU AU46378/99A patent/AU4637899A/en not_active Abandoned
- 1999-07-07 KR KR1020017000376A patent/KR20010083100A/ko not_active Withdrawn
- 1999-07-07 WO PCT/GB1999/002178 patent/WO2000002859A1/en not_active Ceased
- 1999-07-07 CA CA002336806A patent/CA2336806A1/en not_active Abandoned
- 1999-07-07 US US09/743,335 patent/US6365602B1/en not_active Expired - Fee Related
- 1999-07-07 IL IL14077099A patent/IL140770A0/xx unknown
- 1999-07-07 BR BR9912013-5A patent/BR9912013A/pt not_active IP Right Cessation
- 1999-07-07 JP JP2000559090A patent/JP2002520316A/ja active Pending
- 1999-07-08 AR ARP990103362A patent/AR019365A1/es unknown
- 1999-07-09 ID IDP990656D patent/ID24739A/id unknown
-
2001
- 2001-01-09 NO NO20010151A patent/NO20010151L/no not_active Application Discontinuation
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