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1162786

Cl.O=C(CC1CN2CCC1CC2)Nc1cc2ccc(Br)cc2s1
Reaction #84052
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(N)sc2cc(Br)ccc12
Reaction #298340
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Nc2cc(F)ccc2[N+](=O)[O-])sc2cc(Br)ccc12
Reaction #737089
ethyl 6-bromo-2-(5-fluoro-2-nitroanilino)benzo[b]thiophene-3-carboxylate
Ausbeute 77.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Nc2cc(F)ccc2N)sc2cc(Br)ccc12
Reaction #737102
ethyl 6-bromo-2-(2-amino-5-fluoroanilino)benzo[b]thiophene-3-carboxylate
Ausbeute 40.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Nc2cc(F)ccc2N)sc2cc(Br)ccc12
Reaction #737103
ethyl 6-bromo-2-(2-amino-5-fluoroanilino)benzo[b]thiophene-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3ccc(F)cc3Nc3sc4cc(Br)ccc4c32)CC1
Reaction #737123
3-bromo-8-fluoro-12-(4-methylpiperazin-1-yl)-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(N)sc2cc(Br)ccc12
Reaction #907452
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Nc2cc(F)ccc2N)sc2cc(Br)ccc12
Reaction #913104
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Nc2cc(F)ccc2[N+](=O)[O-])sc2cc(Br)ccc12
Reaction #919201
DOI: 10.1039/C8SC04228D
Cl
Reaction #1032889
DOI: 10.1039/C8SC04228D
CN1CCN(C2=Nc3ccc(F)cc3Nc3sc4cc(Br)ccc4c32)CC1
Reaction #1229679
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(N)sc2cc(-c3ccc(F)cc3)ccc12
Reaction #1293073
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Nc2cc(F)ccc2N)sc2cc(Br)ccc12
Reaction #1368961
ethyl 6-bromo-2-(2-amino-5-fluoroanilino)benzo[b]thiophene-3-carboxylate
Ausbeute 40.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Nc2cc(F)ccc2N)sc2cc(Br)ccc12
Reaction #1368962
ethyl 6-bromo-2-(2-amino-5-fluoroanilino)benzo[b]thiophene-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3ccc(F)cc3Nc3sc4cc(Br)ccc4c32)CC1
Reaction #1368989
3-bromo-8-fluoro-12-(4-methylpiperazin-1-yl)-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(CN1CC2CCC1CC2)Nc1cc2ccc(Br)cc2s1
Reaction #1553174
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(N)sc2cc(Br)ccc12
Reaction #1681412
title compound
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(N)sc2cc(-c3ccc(F)cc3)ccc12
Reaction #1681413
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(CC1CN2CCC1CC2)Nc1cc2ccc(Br)cc2s1
Reaction #1983674
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(CC1CN2CCC1CC2)Nc1cc2ccc(Br)cc2s1
Reaction #2075038
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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