Участвует в 477 реакциях

7859

COC(=O)c1c(CBr)nc(-c2ccccc2)nc1-c1cccc([N+](=O)[O-])c1
Reaction #4778
methyl 6-bromomethyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate
Выход 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1ccc(N2CCN(C)C(=O)C2)c2sc(N)nc12
Reaction #8446
4-(2-Amino-4-methoxy-benzothiazol-7-yl)-1-methyl-piperazin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(N(Cc2ccc(C)cc2)Cc2ccc(C)cc2)c2sc(NC(=O)c3ccccc3)nc12
Reaction #8447
N-{7-[Bis-(4-methyl-benzyl)-amino]-4-methoxy-benzothiazol-2-yl}-benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCCN(C)c1ccc(OC)c2nc(N)sc12
Reaction #8448
4-Methoxy-N7-(2-methoxy-ethyl)-N7-methyl-benzothiazole-2,7-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #40695
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
c1cc2nc(c1)CNCCNCCNC2
Reaction #50734
title product
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
NCC(=O)NCc1nncn1-c1ccc(Cl)cc1C(=O)c1ccccc1
Reaction #54221
5-chloro-2-(3-glycylaminomethyl-4H-1,2,4-triazol-4-yl)-benzophenone
Выход 25.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC(=O)NCc1nnc(CCl)n1-c1ccc(Cl)cc1C(=O)c1ccccc1
Reaction #54223
5-chloro-2-(3-acetamidomethyl-5-chloromethyl-4H-1,2,4-triazol-4-yl)-benzophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCCCCCCCCCCCCCOCC(CO)CF
Reaction #62581
title compound ( 11 )
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCc1nc2nc(Br)cc(C)c2[nH]1
Reaction #64377
5-bromo-2-ethyl-7-methylimidazo[4,5-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Br.O=C(CBr)c1ccc2ncccc2c1
Reaction #68604
2-bromo-1-(quinolin-6-yl)ethanone hydrobromide
Выход 76.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1sc(N2CC[C@@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](N)C2)nc1C
Reaction #71818
title compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cc(N2CC[C@H](N)[C@H](OC)C2)sc1C
Reaction #72094
title compound
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1sc(N2CC(CN)C2)nc1C
Reaction #72190
title compound
Выход 60.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Br.NCC(=O)N[C@H]1CCCC[C@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #77832
N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(CBr)C1CCN(C(=O)OCc2ccccc2)CC1
Reaction #158960
4-(2-bromo-acetyl)-piperidine-1-carboxylic acid benzyl ester
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(CBr)c1ccc2c(c1)COc1cc(Br)ccc1-2
Reaction #159097
2-Bromo-1-(3-bromo-6H-benzo[c]chromen-8-yl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)OC[C@H]1O[C@H](Br)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1O[C@H]1O[C@H](COC(C)=O)[C@@H](O[C@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #162027
bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(CBr)C1CCN(C(=O)OCc2ccccc2)CC1
Reaction #166914
4-(2-bromo-acetyl)-piperidine-1-carboxylic acid benzyl ester
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(CBr)c1ccc2c(c1)COc1cc(Br)ccc1-2
Reaction #167043
2-Bromo-1-(3-bromo-6H-benzo[c]chromen-8-yl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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