Substructure Search

49

c1cc2cc(N3CCOCC3)cnc2[nH]1
Reaction #675
Yield 83.6%
c1cc2cc(N3CCOCC3)cnc2[nH]1
Reaction #676
Yield 64.6%
c1cc2cc(N3CCOCC3)cnc2[nH]1
Reaction #677
Yield 90.9%
Nc1cnc2[nH]ccc2c1
Reaction #69138
product
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc2[nH]ccc2c1
Reaction #69783
5-bromo-7-azaindole
Yield 62.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Nc1ccc(F)c(C(O)c2c[nH]c3ncc(Br)cc23)c1F
Reaction #88359
desired compound
Yield 91.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccc([N+](=O)[O-])c1F)c1c[nH]c2ncc(Br)cc12
Reaction #88369
desired compound
Yield 16.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccc(NS(=O)(=O)c2ccccc2F)c1F)c1c[nH]c2ncc(Br)cc12
Reaction #88371
desired compound
Yield 71.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cnc3[nH]cc(C(=O)c4cccc(NS(=O)(=O)c5ccccc5F)c4F)c3c2)cn1
Reaction #88372
desired compound
Yield 25.5%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
COC(=O)c1c(CBr)n(S(=O)(=O)c2ccccc2)c2ncc(Br)cc12
Reaction #88491
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(CN(CC#N)S(=O)(=O)c2ccc(C)cc2)n(S(=O)(=O)c2ccccc2)c2ncc(Br)cc12
Reaction #88492
title compound
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc2c(c1O)c1cc(Br)cnc1n2S(=O)(=O)c1ccccc1
Reaction #88493
title compound
Yield 72.3%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc2c(c1O)c1cccnc1n2S(=O)(=O)c1ccccc1
Reaction #88494
title compound
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc2c(c1Cl)c1cc(Br)cnc1n2S(=O)(=O)c1ccccc1
Reaction #88495
title compound
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1c2cnc(C#N)cc2c2cccnc21
Reaction #88525
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2c(C#N)ncc3c2c2cc(Br)cnc2n3S(=O)(=O)c2ccccc2)CC1
Reaction #88599
title compound
Yield 78.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc2c(c1OC1CCNCC1)c1cc(Br)cnc1n2S(=O)(=O)c1ccccc1
Reaction #88600
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCN1CCC(Oc2c(C#N)ncc3c2c2cc(Br)cnc2n3S(=O)(=O)c2ccccc2)CC1
Reaction #88604
title compound
Yield 92.4%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCN1CCC(Oc2c(C#N)ncc3c2c2cccnc2n3S(=O)(=O)c2ccccc2)CC1
Reaction #88605
title compound
Yield 66.5%DOI: 10.6084/m9.figshare.5104873.v1
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