部分構造検索

Cc1ccc(Nc2ccccn2)cc1

COc1cc(Nc2ccc3c(n2)O[C@H](c2ccccc2)CN(CCO)C3)ccc1C#N
Reaction #363
収率 13.2%
Cc1ccc(Nc2c(C(=O)NOCCO)ccc(=O)n2C)c(F)c1
Reaction #44218
pure desired product
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc(Nc2cc(-c3ccc(Cl)cc3)ccn2)cc1
Reaction #61724
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(Nc2ncc(Cc3ccc(OC)nc3)c3ncccc23)cc1Br
Reaction #77508
5-(3-bromo-4-ethyl-anilino)-8-[(6-methoxy-pyridin-3-yl)-methyl]-[1,6]naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCCc4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #78721
title compound
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCC(=O)c4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #78722
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(N)nc4c(C)cc(C)nc43)cc2)cc1.Cl.Cl
Reaction #78732
title compound
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)Nc1c(C)cc(C)nc1Nc1ccc(CCNC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #78733
N-{[(2-{4-[(4,6-dimethyl-{[(methylamino)carbonothioyl]amino}-2-pyridinyl)amino]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(-n2c(=O)n(C3CC3)c(=O)c3c(Nc4ccc(C#C[Si](C)(C)C)cc4F)n(C)c(=O)c(C)c32)c1
Reaction #162845
N-{3-[3-cyclopropyl-5-(2-fluoro-4-trimethylsilanylethynylphenylamino)-6,8-dimethyl-2,4,7-trioxo-3,4,6,7-tetrahydro-2H-pyrido[4,3-d]pyrimidin-1-yl]phenyl}acetamide
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(Nc2c3c(=O)n(C4CC4)c(=O)n(-c4cccc(NC(C)=O)c4)c3c(C)c(=O)n2C)c(F)c1
Reaction #162846
N-{3-[3-cyclopropyl-5-(4-ethynyl-2-fluorophenylamino)-6,8-dimethyl-2,4,7-trioxo-3,4,6,7-tetrahydro-2H-pyrido[4,3-d]pyrimidin-1-yl]phenyl}acetamide
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](Nc1nc(Nc2ccc(C)cc2)c(C#N)cc1F)C1(NC(=O)OCc2ccccc2)CC1
Reaction #172096
(R)-benzyl 1-(1-(5-cyano-3-fluoro-6-(p-tolylamino)pyridin-2-ylamino)propyl)cyclopropylcarbamate
収率 67.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc2c(c1)C(=O)Nc1cccnc1N2C(=O)NCCN1CCCCC1CN(CC)CC
Reaction #178355
DOI: 10.1039/C8SC04228D
CCC(CC)Oc1cc(C)nc2c1NC(=O)CN2c1c(C)cc(C)cc1C
Reaction #183527
DOI: 10.1039/C8SC04228D
COC(=O)c1cccnc1Nc1ccc(-c2cccc(O)c2)cc1F
Reaction #186834
DOI: 10.1039/C8SC04228D
CCC(CC)Oc1cc(C)nc2c1NCCN2c1c(C)cc(C)cc1C
Reaction #187317
DOI: 10.1039/C8SC04228D
CNc1ncc2cc(-c3c(C)ccc4c(Nc5ccc6c(c5)NCC6(C)C)nccc34)ccc2n1
Reaction #188109
DOI: 10.1039/C8SC04228D
CCC(CC)Oc1cc(C)nc2c1CCCN2c1c(C)cc(C)cc1C
Reaction #200037
DOI: 10.1039/C8SC04228D
NC(=O)c1ccc(N2CCCC(N3CCNC3=O)C2)nc1Nc1ccc(C(=O)N2CCOCC2)cc1
Reaction #206084
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(Nc2nccc3cnccc23)cc1)NC(=O)OC(C)(C)C
Reaction #207578
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(Nc2nc(Cl)ccc2C(N)=O)cc1
Reaction #221573
DOI: 10.1039/C8SC04228D
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