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Brc1ccc(-c2cccnc2)nc1

C[C@H]1CC[C@H](Cn2c(N3CCOC[C@H]3c3ccccc3)nc3c(Br)c(C#N)nc(-c4cncc(Cl)c4)c32)CC1
Reaction #168423
7-bromo-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](Cn2c(N3CCO[C@@H]4CCC[C@H]43)nc3c(Br)c(C#N)nc(-c4cncc(Cl)c4)c32)CC1
Reaction #168428
7-bromo-4-(5-chloropyridin-3-yl)-2-[(4aR,7aR)-hexahydrocyclopenta[b][1,4]oxazin-4(4aH)-yl]-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)nc(-c2cncc(Cl)c2)c2c1nc(N1CCO[C@@H]3CCC[C@H]31)n2C[C@H]1CC[C@H](C)CC1
Reaction #168429
4-(5-chloropyridin-3-yl)-2-[(4aR,7aR)-hexahydrocyclopenta[b][1,4]oxazin-4(4aH)-yl]-7-methyl-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2cncc(C)c2)ncc1Br
Reaction #185996
DOI: 10.1039/C8SC04228D
Brc1ccc(-c2cccnc2)nc1
Reaction #308358
5-bromo-2,3′-bipyridine
Ausbeute 70.6%DOI: 10.6084/m9.figshare.5104873.v1
c1cncc(-c2ccc(-c3c4ccccc4c(-c4ccc(-c5cccnc5)nc4)c4ccccc34)cn2)c1
Reaction #308359
9,10-bis(2,3′-bipyridine-5-yl)anthracene
DOI: 10.6084/m9.figshare.5104873.v1
c1cncc(-c2ccc(-c3ccc4c(c3)c3cc(-c5ccc(-c6cccnc6)nc5)ccc3n4-c3cccc4ccccc34)cn2)c1
Reaction #308363
3,6-bis(2,3′-bipyridine-5-yl)-9-naphthalene-1-yl-carbazole
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC1(CCCCCC)c2cc(-c3ccc(-c4cccnc4)nc3)ccc2-c2ccc(-c3ccc(-c4cccnc4)nc3)cc21
Reaction #308364
2,7-bis(2,3′-bipyridine-5-yl)-9,9-dihexylfluorene
Ausbeute 32.8%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(-c2cnc3ccccc3c2)nc1
Reaction #470384
white solid
Ausbeute 107.4%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(-c2cnc3ccccc3c2)nc1
Reaction #470386
white solid
Ausbeute 107.4%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc(-c2cccnc2)cc1Cc1ccccc1
Reaction #1446481
target compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncccc1-c1ccc(Br)cn1
Reaction #1493098
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ncc(Br)cc2N)cn1
Reaction #1518728
5-Bromo-6′-methoxy-2,3′-bipyridin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ncc(Br)cc2Nc2c(C)c(-c3ccccn3)nc3cc(F)cc(F)c23)cn1
Reaction #1518729
N-(5-bromo-6′-methoxy-2,3′-bipyridin-3-yl)-5,7-difluoro-3-methyl-2-(pyridin-2-yl)-quinolin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nccc(N3CCOCC3)c2Nc2c(C)c(-c3ccccn3)nc3cc(F)cc(F)c23)cn1
Reaction #1518730
5,7-difluoro-N-(6′-methoxymorpholino-2,3′-bipyridin-3-yl)-3-methyl-2-(pyridin-2-yl)quinolin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ncc(Br)cc2[N+](=O)[O-])cn1
Reaction #1518745
5-bromo-6′-methoxy-3-nitro-2,3′-bipyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ncc(Br)cc2N)cn1
Reaction #1518746
5-Bromo-6′-methoxy-2,3′-bipyridin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ncc(N3CCOCC3)cc2N)cn1
Reaction #1518747
6′-methoxy-5-morpholino-2,3′-bipyridin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncccc1-c1ccc(Br)cn1
Reaction #1710031
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncccc1-c1ccc(Br)cn1
Reaction #1835296
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
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