CN102227429B - 作为趋化因子受体调节剂的3-氨基环戊烷羧酰胺 - Google Patents
作为趋化因子受体调节剂的3-氨基环戊烷羧酰胺 Download PDFInfo
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- CN102227429B CN102227429B CN200980147183.7A CN200980147183A CN102227429B CN 102227429 B CN102227429 B CN 102227429B CN 200980147183 A CN200980147183 A CN 200980147183A CN 102227429 B CN102227429 B CN 102227429B
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- Prior art keywords
- trifluoromethyl
- amino
- carbonyl
- diazabicyclo
- anhydro
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- 0 CCC*(C(CC1)CC1(C(*(CC1*(C2)C(C)=**)C2C1=C)=O)*(C)=C)C(C(C)(C)C(*)(C(C)C)*=C1*(C)CC)C1(*1CC1)O* Chemical compound CCC*(C(CC1)CC1(C(*(CC1*(C2)C(C)=**)C2C1=C)=O)*(C)=C)C(C(C)(C)C(*)(C(C)C)*=C1*(C)CC)C1(*1CC1)O* 0.000 description 4
- MCOPMLXHPNYMPU-XJJIGLNASA-N CC(C)(C)OC(N(C[C@@H]1C2)[C@@H]2CN1C([C@@](CC1)(C[C@@H]1N([C@@H](CCOC1)[C@@H]1OC)C(C(F)(F)F)=O)C(C)(C)O)=O)=O Chemical compound CC(C)(C)OC(N(C[C@@H]1C2)[C@@H]2CN1C([C@@](CC1)(C[C@@H]1N([C@@H](CCOC1)[C@@H]1OC)C(C(F)(F)F)=O)C(C)(C)O)=O)=O MCOPMLXHPNYMPU-XJJIGLNASA-N 0.000 description 1
- NJORUBSEKQXPEW-WUZPWTHYSA-N CC(C)(C)OC(N(C[C@@H]1C2)[C@@H]2CN1C([C@@](CC1)(C[C@@H]1N([C@@H](CCOC1)[C@@H]1OC)C(C(F)(F)F)=O)C1(CCC1)OC(C)=O)=O)=O Chemical compound CC(C)(C)OC(N(C[C@@H]1C2)[C@@H]2CN1C([C@@](CC1)(C[C@@H]1N([C@@H](CCOC1)[C@@H]1OC)C(C(F)(F)F)=O)C1(CCC1)OC(C)=O)=O)=O NJORUBSEKQXPEW-WUZPWTHYSA-N 0.000 description 1
- OAKHTXKDPQXCIC-KKPNGEORSA-N CC(C)(C)OC(N(C[C@H]1N(C2)c3nccc(C(F)(F)F)c3)[C@H]2C1O)=O Chemical compound CC(C)(C)OC(N(C[C@H]1N(C2)c3nccc(C(F)(F)F)c3)[C@H]2C1O)=O OAKHTXKDPQXCIC-KKPNGEORSA-N 0.000 description 1
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- RJNNXWKWUCMJGB-MQMGHXAXSA-N CC(C)([C@](CC1)(C[C@@H]1N[C@@H](CCOC1)[C@@H]1OC)C(N(C[C@@H]1C2)[C@@H]2CN1c1cc(C(F)(F)F)ncc1)=O)O Chemical compound CC(C)([C@](CC1)(C[C@@H]1N[C@@H](CCOC1)[C@@H]1OC)C(N(C[C@@H]1C2)[C@@H]2CN1c1cc(C(F)(F)F)ncc1)=O)O RJNNXWKWUCMJGB-MQMGHXAXSA-N 0.000 description 1
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- AYGHWHNGAHYUKL-YFJVBQAUSA-N CC(C)[C@](CC1)(C[C@@H]1/C=N/[C@@H](CCOC1)[C@@H]1OC)C(N(C[C@@H]1C2)[C@@H]2CN1c1cc(C(F)(F)F)nc(C(F)(F)F)c1)=O Chemical compound CC(C)[C@](CC1)(C[C@@H]1/C=N/[C@@H](CCOC1)[C@@H]1OC)C(N(C[C@@H]1C2)[C@@H]2CN1c1cc(C(F)(F)F)nc(C(F)(F)F)c1)=O AYGHWHNGAHYUKL-YFJVBQAUSA-N 0.000 description 1
- YRRHRDDUJDWJNS-GKNGNAOLSA-N CO[C@H](COCC1)[C@H]1N[C@H](CC1)C[C@@]1(C(C(F)(F)F)O)C(N(C[C@@H]1C2)[C@@H]2CN1c1ccnc(C(F)(F)F)n1)=O Chemical compound CO[C@H](COCC1)[C@H]1N[C@H](CC1)C[C@@]1(C(C(F)(F)F)O)C(N(C[C@@H]1C2)[C@@H]2CN1c1ccnc(C(F)(F)F)n1)=O YRRHRDDUJDWJNS-GKNGNAOLSA-N 0.000 description 1
- QDOADAPYFMASTQ-VHFSTGMOSA-N CO[C@H](COCC1)[C@H]1N[C@H](CC1)C[C@H]1C(N(C[C@@H]1C2)[C@@H]2CN1c1nccc(C(F)(F)F)c1)=O Chemical compound CO[C@H](COCC1)[C@H]1N[C@H](CC1)C[C@H]1C(N(C[C@@H]1C2)[C@@H]2CN1c1nccc(C(F)(F)F)c1)=O QDOADAPYFMASTQ-VHFSTGMOSA-N 0.000 description 1
- NLITZQDXQNVFEB-RGKOJQFUSA-N CO[C@H]1[C@@H](CCC[C@H](CC2)C[C@@]2(CC(F)F)C(N(C[C@@H]2C3)[C@@H]3CN2c2nc(C(F)(F)F)ccc2)=O)CCOC1 Chemical compound CO[C@H]1[C@@H](CCC[C@H](CC2)C[C@@]2(CC(F)F)C(N(C[C@@H]2C3)[C@@H]3CN2c2nc(C(F)(F)F)ccc2)=O)CCOC1 NLITZQDXQNVFEB-RGKOJQFUSA-N 0.000 description 1
- SSTIDYXGQYDDDZ-ZBIJSRSNSA-N CO[C@H]1[C@@H](CCC[C@H](CC2)C[C@@]2(CC(F)F)C(N(C[C@@H]2C3)[C@@H]3CN2c2nc(C(F)(F)F)ncc2)=O)CCOC1 Chemical compound CO[C@H]1[C@@H](CCC[C@H](CC2)C[C@@]2(CC(F)F)C(N(C[C@@H]2C3)[C@@H]3CN2c2nc(C(F)(F)F)ncc2)=O)CCOC1 SSTIDYXGQYDDDZ-ZBIJSRSNSA-N 0.000 description 1
- KZWTVSPHZPRNRJ-SKZKBGNNSA-N C[C@H](COCC1)[C@H]1N[C@H](CC1)C[C@@]1(C(C)(C)O)C(N(C[C@@H]1C2)[C@@H]2CN1c1ccnc(C(F)(F)F)n1)=O Chemical compound C[C@H](COCC1)[C@H]1N[C@H](CC1)C[C@@]1(C(C)(C)O)C(N(C[C@@H]1C2)[C@@H]2CN1c1ccnc(C(F)(F)F)n1)=O KZWTVSPHZPRNRJ-SKZKBGNNSA-N 0.000 description 1
- IFDGSTIIEXETJZ-SZBHIRRCSA-N OC([C@@H](C1)NC2)[C@@H]2N1c1nccc(C(F)(F)F)c1 Chemical compound OC([C@@H](C1)NC2)[C@@H]2N1c1nccc(C(F)(F)F)c1 IFDGSTIIEXETJZ-SZBHIRRCSA-N 0.000 description 1
- HGYIBUDJAODOHS-XFKKCKKNSA-N OC1[C@@H]2N(Cc3ccccc3)C[C@H]1NC2 Chemical compound OC1[C@@H]2N(Cc3ccccc3)C[C@H]1NC2 HGYIBUDJAODOHS-XFKKCKKNSA-N 0.000 description 1
Classifications
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- 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
- C07D487/02—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 two hetero rings
- C07D487/08—Bridged systems
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Vascular Medicine (AREA)
- Otolaryngology (AREA)
- Transplantation (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11805308P | 2008-11-26 | 2008-11-26 | |
| US61/118,053 | 2008-11-26 | ||
| PCT/IB2009/055232 WO2010061329A1 (en) | 2008-11-26 | 2009-11-20 | 3-aminocyclopentanecarboxamides as chemokine receptor modulators |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102227429A CN102227429A (zh) | 2011-10-26 |
| CN102227429B true CN102227429B (zh) | 2014-05-28 |
Family
ID=41693100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980147183.7A Expired - Fee Related CN102227429B (zh) | 2008-11-26 | 2009-11-20 | 作为趋化因子受体调节剂的3-氨基环戊烷羧酰胺 |
Country Status (38)
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2743030C (en) * | 2008-11-26 | 2013-10-22 | Pfizer Inc. | 3-aminocyclopentanecarboxamides as chemokine receptor modulators |
| KR101303963B1 (ko) * | 2011-04-08 | 2013-09-05 | 재단법인 경기과학기술진흥원 | (1ｒ,2ｒ,3ｒ)-3-아미노사이클로펜탄-1,2-디올을 포함하는 항알러지용 조성물 |
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| WO2016010131A1 (ja) * | 2014-07-17 | 2016-01-21 | 参天製薬株式会社 | 加齢黄斑変性の予防または治療剤 |
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