部分構造検索

Nc1ccc(Br)cc1N

CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCc3ccccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4091
N-[5-bromo-2-(2,3-dihydro-1H-indol-1-yl)phenyl]-4-methyl-1-piperazinecarboxamide maleate
収率 39.8%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)N=C(N1CCN(c3ccccc3)CC1)c1cccc3c1N2CC3
Reaction #4105
product
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)N=C(N1CCN(Cc3ccccc3)CC1)c1cccc3c1N2CC3
Reaction #4106
9-Bromo-6-(4-phenylmethyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(C2=Nc3cc(Br)ccc3N3CCc4cccc2c43)CC1
Reaction #4108
9-Bromo-6-(4-ethoxycarbonyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1Br)N1CCc3cccc(c31)C(N1CCN(C)CC1)=N2
Reaction #4128
product
収率 11.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4133
product
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3-n3ccc4cc(Br)cc2c43)CC1
Reaction #4134
product
収率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCc3ccccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4149
N-[5-bromo-2-(2,3-dihydro-1H-indol-1-yl)phenyl]-4-methyl-1-piperazinecarboxamide maleate
収率 39.8%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)N=C(N1CCN(c3ccccc3)CC1)c1cccc3c1N2CC3
Reaction #4163
product
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)N=C(N1CCN(Cc3ccccc3)CC1)c1cccc3c1N2CC3
Reaction #4164
9-Bromo-6-(4-phenylmethyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(C2=Nc3cc(Br)ccc3N3CCc4cccc2c43)CC1
Reaction #4166
9-Bromo-6-(4-ethoxycarbonyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1Br)N1CCc3cccc(c31)C(N1CCN(C)CC1)=N2
Reaction #4186
product
収率 11.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4191
product
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3-n3ccc4cc(Br)cc2c43)CC1
Reaction #4192
product
収率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2cc(Br)cc(N)c21
Reaction #5023
compound
収率 32.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2cc(Br)cc(C#N)c21
Reaction #5024
compound
収率 81.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc(N)c([N+](=O)[O-])cc2Br)cc1
Reaction #41619
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1cc([N+](=O)[O-])c(N)cc1Oc1ccc(S(C)(=O)=O)cc1
Reaction #41620
t-butyl 2-(4-amino-2-(4-methanesulfonyl-phenoxy)-5-nitro-phenyl)-pyrrole-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCc3cc(Br)cc(N)c32)cc1
Reaction #46974
compound 18
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCc3cccc(N)c32)cc1
Reaction #46975
compound 19
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
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