CN101910152B - 作为janus激酶抑制剂的4-吡唑基-n-芳基嘧啶-2-胺和4-吡唑基-n-杂芳基嘧啶-2-胺 - Google Patents
作为janus激酶抑制剂的4-吡唑基-n-芳基嘧啶-2-胺和4-吡唑基-n-杂芳基嘧啶-2-胺 Download PDFInfo
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- CN101910152B CN101910152B CN200880123789.2A CN200880123789A CN101910152B CN 101910152 B CN101910152 B CN 101910152B CN 200880123789 A CN200880123789 A CN 200880123789A CN 101910152 B CN101910152 B CN 101910152B
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- pyrimidine
- amino
- pyrazol
- phenyl
- cyclopentyl
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- 0 CC[n]1nc(*)c(-c2nc(NC3=CC=CC(C)C=C3)nc(**)c2*)c1C Chemical compound CC[n]1nc(*)c(-c2nc(NC3=CC=CC(C)C=C3)nc(**)c2*)c1C 0.000 description 6
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- IPUHOAZPUHAFAG-UHFFFAOYSA-N CCS(N(C1)CC1(CC#N)[n]1ncc(-c2nc(Nc(cc3)ccc3C(N(CC3)CCC3OC)=O)ncc2)c1)(=O)=O Chemical compound CCS(N(C1)CC1(CC#N)[n]1ncc(-c2nc(Nc(cc3)ccc3C(N(CC3)CCC3OC)=O)ncc2)c1)(=O)=O IPUHOAZPUHAFAG-UHFFFAOYSA-N 0.000 description 1
- QZTTVFJXTAGTRG-UHFFFAOYSA-N CCS(N(C1)CC1(CC#N)[n]1ncc(-c2nc(Nc(cc3)ccc3C(N3CCOCC3)=O)ncc2)c1)(=O)=O Chemical compound CCS(N(C1)CC1(CC#N)[n]1ncc(-c2nc(Nc(cc3)ccc3C(N3CCOCC3)=O)ncc2)c1)(=O)=O QZTTVFJXTAGTRG-UHFFFAOYSA-N 0.000 description 1
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- HYJZBEYSEQHUAG-UHFFFAOYSA-N CN(C)C(c(cc1)ccc1Nc1nc(-c2c[n](C(CC(CC3)CCN3C(c(ccc(F)c3)c3F)=O)CC#N)nc2)ccn1)=O Chemical compound CN(C)C(c(cc1)ccc1Nc1nc(-c2c[n](C(CC(CC3)CCN3C(c(ccc(F)c3)c3F)=O)CC#N)nc2)ccn1)=O HYJZBEYSEQHUAG-UHFFFAOYSA-N 0.000 description 1
- CTHDAGOBRACITE-UHFFFAOYSA-N CN(C1)N(C(CC#N)C2CCCC2)C=C1c1nc(Nc(cc2)ccc2C(N2CCCC2)=O)ncc1 Chemical compound CN(C1)N(C(CC#N)C2CCCC2)C=C1c1nc(Nc(cc2)ccc2C(N2CCCC2)=O)ncc1 CTHDAGOBRACITE-UHFFFAOYSA-N 0.000 description 1
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- JPXDQJBWCIPWEI-UHFFFAOYSA-N N#CCC(C1)(CC1C#N)[n]1ncc(-c2ccnc(Nc(cc3)ccc3N(CCOC3)C3=O)n2)c1 Chemical compound N#CCC(C1)(CC1C#N)[n]1ncc(-c2ccnc(Nc(cc3)ccc3N(CCOC3)C3=O)n2)c1 JPXDQJBWCIPWEI-UHFFFAOYSA-N 0.000 description 1
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- REJYYOPUBDCFHH-UHFFFAOYSA-N N#CCC(C1CCCC1)[n]1ncc(-c2ccnc(Nc(cc3)ccc3NC(CNCC3CCOCC3)=O)n2)c1 Chemical compound N#CCC(C1CCCC1)[n]1ncc(-c2ccnc(Nc(cc3)ccc3NC(CNCC3CCOCC3)=O)n2)c1 REJYYOPUBDCFHH-UHFFFAOYSA-N 0.000 description 1
- OLHBLPFMECINKZ-UHFFFAOYSA-N N#CCC(C1CCCC1)[n]1ncc(-c2ccnc(Nc3cccc(-c4cnc[o]4)c3)n2)c1 Chemical compound N#CCC(C1CCCC1)[n]1ncc(-c2ccnc(Nc3cccc(-c4cnc[o]4)c3)n2)c1 OLHBLPFMECINKZ-UHFFFAOYSA-N 0.000 description 1
- PWYRKGARXFZNFG-UHFFFAOYSA-N N#CCC(C1CCCC1)[n]1ncc(-c2ccnc(Nc3cccc(C(N(CC4)CCC4c4ccccc4)=O)c3)n2)c1 Chemical compound N#CCC(C1CCCC1)[n]1ncc(-c2ccnc(Nc3cccc(C(N(CC4)CCC4c4ccccc4)=O)c3)n2)c1 PWYRKGARXFZNFG-UHFFFAOYSA-N 0.000 description 1
- SAHKRSGAQBBMNF-XQZUBTRRSA-N N#CCC(C1CCCC1)[n]1ncc(-c2ccnc(Nc3cccc(NC(CN(CC4)C[C@@H]4O)=O)c3)n2)c1 Chemical compound N#CCC(C1CCCC1)[n]1ncc(-c2ccnc(Nc3cccc(NC(CN(CC4)C[C@@H]4O)=O)c3)n2)c1 SAHKRSGAQBBMNF-XQZUBTRRSA-N 0.000 description 1
- BGVPSFNBSPRWGM-UHFFFAOYSA-N N#CCC(C1CCCC1)[n]1ncc(-c2nc(Nc(cc3)ccc3C(NCC3CCOCC3)=O)ncc2)c1 Chemical compound N#CCC(C1CCCC1)[n]1ncc(-c2nc(Nc(cc3)ccc3C(NCC3CCOCC3)=O)ncc2)c1 BGVPSFNBSPRWGM-UHFFFAOYSA-N 0.000 description 1
- JEWXHSQGKQLDBY-UHFFFAOYSA-N N#CCC(C1CCCC1)[n]1ncc(-c2nc(Nc(cc3)ccc3NC(CN3CCCC3)=O)ncc2)c1 Chemical compound N#CCC(C1CCCC1)[n]1ncc(-c2nc(Nc(cc3)ccc3NC(CN3CCCC3)=O)ncc2)c1 JEWXHSQGKQLDBY-UHFFFAOYSA-N 0.000 description 1
- BPRQLCUFFJIKQQ-UHFFFAOYSA-N N#CCC(C1CCCC1)[n]1ncc(-c2nc(Nc3cccc(C(N(CC4)CCC4Oc4ccccc4)=O)c3)ncc2)c1 Chemical compound N#CCC(C1CCCC1)[n]1ncc(-c2nc(Nc3cccc(C(N(CC4)CCC4Oc4ccccc4)=O)c3)ncc2)c1 BPRQLCUFFJIKQQ-UHFFFAOYSA-N 0.000 description 1
- IYQUBKWBCUCNIX-UHFFFAOYSA-N N#CCC(CC(CC1)CCN1C(c(ccc(F)c1)c1F)=O)[n]1ncc(-c2ccnc(Nc(cc3)ccc3N3CCOCC3)n2)c1 Chemical compound N#CCC(CC(CC1)CCN1C(c(ccc(F)c1)c1F)=O)[n]1ncc(-c2ccnc(Nc(cc3)ccc3N3CCOCC3)n2)c1 IYQUBKWBCUCNIX-UHFFFAOYSA-N 0.000 description 1
- NGDKYIYRDABPGP-UHFFFAOYSA-N N=C(c1cccc(Nc2nc(-c3c[n](C(CC#N)C4CCCC4)nc3)ccn2)c1)N1CCOCC1 Chemical compound N=C(c1cccc(Nc2nc(-c3c[n](C(CC#N)C4CCCC4)nc3)ccn2)c1)N1CCOCC1 NGDKYIYRDABPGP-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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| US98860607P | 2007-11-16 | 2007-11-16 | |
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| PCT/US2008/083319 WO2009064835A1 (en) | 2007-11-16 | 2008-11-13 | 4-pyrazolyl-n-arylpyrimidin-2-amines and 4-pyrazolyl-n-heteroarylpyrimidin-2-amines as janus kinase inhibitors |
Publications (2)
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| CN101910152A CN101910152A (zh) | 2010-12-08 |
| CN101910152B true CN101910152B (zh) | 2014-08-06 |
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| ZA201004055B (en) | 2012-09-26 |
| IL205571A (en) | 2015-09-24 |
| BRPI0820544A2 (pt) | 2015-06-16 |
| JP2011503194A (ja) | 2011-01-27 |
| KR101580482B1 (ko) | 2015-12-28 |
| EA201070618A1 (ru) | 2010-12-30 |
| EA020777B1 (ru) | 2015-01-30 |
| UA104849C2 (uk) | 2014-03-25 |
| CR11430A (es) | 2010-07-01 |
| EP2220068A1 (en) | 2010-08-25 |
| ECSP10010263A (es) | 2010-07-30 |
| KR20100095582A (ko) | 2010-08-31 |
| AU2008321046B2 (en) | 2013-10-24 |
| HK1147476A1 (zh) | 2011-08-12 |
| NZ585139A (en) | 2012-05-25 |
| CA2704599C (en) | 2015-05-12 |
| AU2008321046A1 (en) | 2009-05-22 |
| US8309718B2 (en) | 2012-11-13 |
| CO6280420A2 (es) | 2011-05-20 |
| US20090318405A1 (en) | 2009-12-24 |
| EP2220068B1 (en) | 2016-01-27 |
| MX2010005300A (es) | 2010-06-25 |
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