Substructure Search

216065

CN1C(=O)CCC1c1cncc(Br)c1
Reaction #1140
5-bromo-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Br)cc2CCC1Br
Reaction #46132
3,7-dibromo-1,3,4,5-tetrahydro-1-benzazepin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(Br)C(=O)NCCS(=O)(=O)[O-].[Na+]
Reaction #52577
Sodium 2-(2-bromopropionylamino)-ethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O.O=C1Cc2cccnc2N1
Reaction #52599
7-azaoxindole acetic acid salt
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O.O=C1Cc2cccnc2N1
Reaction #52679
7-aza-2-oxindole acetic acid salt
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)[C@H](C(=O)O)N2C(=O)C(Br)(Br)[C@H]2S1(=O)=O
Reaction #62971
6,6-dibromopenicillanic acid 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)[C@H](C(=O)O)N2C(=O)C[C@H]2S1(=O)=O
Reaction #62972
penicillanic acid 1,1-dioxide
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(CSC(C)(C)C)C(=O)[C@@H](Br)CO)cc1
Reaction #93718
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(CSC(C)(C)C)C(=O)[C@@H](Br)[C@@H](C)O)cc1
Reaction #93720
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(Br)C(=O)Nc1ccc(C(F)(F)F)cc1
Reaction #183576
DOI: 10.1039/C8SC04228D
O=C1Nc2ccccc2CCC1Oc1ccc([N+](=O)[O-])c(OCc2ccccc2)c1
Reaction #187822
DOI: 10.1039/C8SC04228D
CC(=O)OC(c1ccc2nc3n(c2c1)CCCS3)C1(Br)C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=CSC21
Reaction #198639
DOI: 10.1039/C8SC04228D
CC#CC(C)(C)NC(=O)C(CC)Oc1cnc(Cl)c(Cl)c1
Reaction #205477
DOI: 10.1039/C8SC04228D
Cc1cc(Br)ccc1NC(=O)C(C)(Br)C(=O)O
Reaction #208520
DOI: 10.1039/C8SC04228D
COc1ccc(CCCC(Br)C(=O)N2C(=O)OCC2Cc2ccccc2)cc1
Reaction #211647
DOI: 10.1039/C8SC04228D
CC1(C)S[C@H]2N(C(=O)C2(Br)Br)C1C(=O)OCc1ccccc1
Reaction #214748
title product
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCC2=C1CC(Br)C(=O)N2
Reaction #214892
bromo-3,4,5,6,7,8-hexahydrocarbostyril-5-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2c(sc(NC(=O)C(C)Br)c2C(=O)c2ccccc2Cl)C1
Reaction #216673
intended product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2c(sc(NC(=O)C(C)N)c2C(=O)c2ccccc2Cl)C1
Reaction #216674
intended compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCCOC(=O)N1CCc2c(sc(NC(=O)C(C)Br)c2C(=O)c2ccccc2Cl)C1
Reaction #216680
intended compound
Yield 65.4%DOI: 10.6084/m9.figshare.5104873.v1
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