Substructure Search

58680

Br.Nc1ncc(Br)cc1CO
Reaction #46490
title compound
Yield 161.9%DOI: 10.6084/m9.figshare.5104873.v1
Br.Nc1ncc(Br)cc1CBr
Reaction #46491
title compound
Yield 172.4%DOI: 10.6084/m9.figshare.5104873.v1
CNCc1cc(Br)cnc1N
Reaction #46492
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)cnc1N
Reaction #46532
title compound
Yield 98.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ncc(Br)cc2CC1N=C(c1ccccc1)c1ccccc1
Reaction #46576
title compound
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCNCc1cc(Br)cnc1N
Reaction #46585
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCN1Cc2cc(Br)cnc2NC1=O
Reaction #46586
title compound
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)C#Cc1cc(Br)cnc1N
Reaction #69782
4-(2-amino-5-bromo-pyridin-3-yl)-2-methyl-but-3-yn-2-ol
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #88489
solid
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2cc(Br)cnc2[nH]1
Reaction #88490
title compound
Yield 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCc1nc2c(c(C)c1Br)CCN2C
Reaction #88670
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCc1nc2c(c(C)c1OC(C)=O)CCN2C
Reaction #88671
2a
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCc1nc2c(c(C)c1Br)CCN2C
Reaction #88674
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCc1nc2c(c(C)c1OC(C)=O)CCN2C
Reaction #88675
2b
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCc1nc2c(c(C)c1Br)CCN2C
Reaction #88684
5-bromo-1,4-dimethyl-6-octyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCc1nc2c(c(C)c1OC(C)=O)CCN2C
Reaction #88685
1d
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(c2cc(Br)cnc2NN)OC1(C)C
Reaction #90355
5-bromo-2-hydrazinyl-3-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)cnc1Nc1ncc2c3ccncc3n(C3CCCC3)c2n1
Reaction #166301
N-(5-bromo-3-methyl-2-pyridinyl)-9-cyclopentyl-9H-pyrido[4′,3′:4,5]pyrrolo[2,3-d]pyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCN(C(=O)OC(C)(C)C)CC2)cnc1Nc1ncc2c3ccncc3n(C3CCCC3)c2n1
Reaction #166302
compound 78
Yield 53.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(-c2cnc(N3CCN(C(C)C)CC3)c(C)c2)c1
Reaction #168101
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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