Teilstruktursuche

1251183

Cl.Cl.O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1cc(Cl)cnc1F
Reaction #41071
title compound
Ausbeute 6.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](Cn2c(N3CCOC[C@H]3c3ccccc3)nc3cc(Cl)nc(-c4cncc(Cl)c4)c32)CC1
Reaction #168282
6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](Cn2cnc3cc(Cl)nc(-c4cncc(Cl)c4)c32)CC1
Reaction #168287
6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC([C@H]1CC[C@H](C)CC1)n1cnc2cc(Cl)nc(-c3cncc(Cl)c3)c21
Reaction #168391
racemic 6-chloro-4-(5-chloropyridin-3-yl)-3-[1-(trans-4-methylcyclohexyl)ethyl]-3H-imidazo[4,5-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(Cn2c(N3CCO[C@@H]4CCC[C@H]43)nc3cc(Cl)nc(-c4cncc(Cl)c4)c32)cc1
Reaction #168447
6-chloro-4-(5-chloropyridin-3-yl)-2-[(trans)-hexahydrocyclopenta[b][1,4]oxazin-4(4aH)-yl]-3-[4-(trifluoromethyl)benzyl]-3H-imidazo[4,5-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](Cn2c(N3CCO[C@@H]4CCC[C@H]43)nc3cc(Cl)nc(-c4cc(Cl)cnc4F)c32)CC1
Reaction #168450
6-chloro-4-(5-chloro-2-fluoropyridin-3-yl)-2-[(trans)-hexahydrocyclopenta[b][1,4]oxazin-4(4aH)-yl]-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](Cn2c(N3CCO[C@@H]4CCC[C@H]43)nc3cc(Cl)nc(-c4cc(Cl)cnc4OCc4ccccc4)c32)CC1
Reaction #168457
4-[2-(benzyloxy)-5-chloropyridin-3-yl]-6-chloro-2-[(trans)-hexahydrocyclopenta[b][1,4]oxazin-4(4aH)-yl]-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CSC(Oc2ccc(-c3cncc(Cl)c3)nc2)C(OC(C)=O)C1OC(C)=O
Reaction #191895
DOI: 10.1039/C8SC04228D
COCCNc1nc(C)nc(-c2cc(Cl)cnc2F)n1
Reaction #210787
DOI: 10.1039/C8SC04228D
COc1ccc(CN(Cc2ccc(OC)cc2)c2nc(C)nc(-c3cc(Cl)cnc3F)n2)cc1
Reaction #228160
DOI: 10.1039/C8SC04228D
CC1=NC2(N=C1N)c1cc(-c3cncc(Cl)c3)ccc1CC21CCC1
Reaction #229006
DOI: 10.1039/C8SC04228D
CC(c1ccc(-c2cncc(Cl)c2)cc1)N1CCC(CCCO)(c2ccc(F)cc2)OC1=O
Reaction #233883
DOI: 10.1039/C8SC04228D
COc1ccc(CN(Cc2ccc(OC)cc2)c2nc(C)nc(-c3cc(Cl)cnc3F)n2)cc1
Reaction #245074
DOI: 10.1039/C8SC04228D
Cc1nn(C)c(C)c1-n1c(=O)n(C)c2cnc3ccc(-c4cnc(N)c(Cl)c4)cc3c21
Reaction #384156
DOI: 10.1039/C8SC04228D
Cc1oc(-c2cncc(Cl)c2)cc1C=O
Reaction #392289
DOI: 10.1039/C8SC04228D
CS(=O)(=O)NC(=O)c1cc(Cl)c(Cc2cnc(C3CC3)c(Cl)c2)cc1F
Reaction #398186
DOI: 10.1039/C8SC04228D
CS(=O)(=O)N1CCN(Cc2cc3c(N4CCOCC4)nc(-c4cnc(N)c(Cl)c4)nc3s2)CC1
Reaction #478271
376
Ausbeute 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCN(Cc2cc3nc(-c4cnc(N)c(Cl)c4)nc(N4CCOCC4)c3s2)CC1
Reaction #478272
377
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #507012
solid
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ncc(-c2ccc3ncc4c(c3c2)n(-c2cn(C)nc2C)c(=O)n4C)cc1Cl
Reaction #532879
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter