Substructure Search

CBr

COc1cc2c(cc1OC1(C3CCN(CCNC=O)C3)C=CC=CN1)nc(Nc1ccc(Br)c(C)c1)n2C
Reaction #41774
4-(2-{[4-bromo-3-methylphenyl]amino-6-methoxy-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CC(C)c4cccc(Br)c4)CC3)cccc2n1
Reaction #44121
title compound
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(F)c(CCN2CCN(c3cccc4nc(C)ccc34)CC2)c1
Reaction #44145
title compound
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(Br)ccc4F)CC3)cccc2n1
Reaction #44146
title compound
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(NC(=O)C(C)(C)C)ccc4F)CC3)cccc2n1
Reaction #44147
title compound
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(NS(C)(=O)=O)ccc4F)CC3)cccc2n1
Reaction #44148
title compound
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(N5CCNC5=O)ccc4F)CC3)cccc2n1
Reaction #44149
title compound
Yield 35.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)NCc1cc(Oc2ccc3c(ccn3C(=O)Nc3ccc(F)c(C(F)(F)F)c3)c2)ncn1
Reaction #73412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1Cc1cc(Oc2ccc3c(ccn3C(=O)Nc3ccc(F)c(C(F)(F)F)c3)c2)ncn1
Reaction #73413
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc(C(=O)C(OC)c3ccc(N4CCOCC4)cc3)n2)cc(OC)c1Br
Reaction #84772
1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #84868
product
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #84871
product
Yield 14.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1n(-c2cccc(Br)c2)cnn1C(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #157480
4-(3-bromophenyl)-2-(triphenylmethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(SC(F)(F)F)nc1)c1cnc(N2CC[C@@H](O)C2)c(Br)c1
Reaction #160986
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(SC(F)(F)F)nc1)c1cnc(Cl)c(Br)c1
Reaction #160987
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(Oc1ccc(OCC(=O)OCC)c(CC)c1)c1cccc(Br)n1
Reaction #180593
DOI: 10.1039/C8SC04228D
COc1cccc(C(=O)N2c3cc(Br)ccc3-n3cccc3C2C(C)(C)C)c1
Reaction #182358
DOI: 10.1039/C8SC04228D
CC=Cc1cc(C(OCc2ccccc2)(C(F)(F)F)C(F)(F)F)ccc1N1CCN(C(=O)CN2C(=O)NC(C)(c3cnc4c(c3)OCCO4)C2=O)CC1
Reaction #182450
DOI: 10.1039/C8SC04228D
Cc1ccc2c(N3CCN(CCc4cc(NS(C)(=O)=O)ccc4F)CC3)cccc2n1
Reaction #183493
DOI: 10.1039/C8SC04228D
COc1ccc(Br)cc1C(C)(C)CC(=O)C(=O)O
Reaction #186313
DOI: 10.1039/C8SC04228D
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