N-chlorosuccinimide

CN(C)S(=O)(=O)c1c(S(N)(=O)=O)c(C(C)(C)C)cn1C
Reaction #919
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSCc1c(N)c(F)cc(F)c1F
Reaction #1366
2-methylthiomethyl-3,4,6-trifluoroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1nc(-c2ccccc2)[nH]c(=O)c1Cl
Reaction #1545
5-chloro-6-ethyl-2-phenyl-4(3H)-pyrimidinone
Ausbeute 87.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2Cc3ccc(Cl)n3Cc3ccccc32)cc1
Reaction #3597
desired product
Ausbeute 68.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2Cc3ccc(Cl)n3-c3ccccc32)cc1
Reaction #3598
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(N)c(Cl)c1
Reaction #3680
ethyl 3-chloro-4-aminobenzoate
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(CCl)(OCC)OCC
Reaction #4016
2-chloro-1,1,1-triethoxyethane
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
ClCc1cc2ccccc2nc1I
Reaction #5221
3-chloromethyl-2-iodoquinoline
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
ClCc1cc2ccccc2nc1I
Reaction #6323
3-chloromethyl-2-iodoquinoline
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCc1nc(Cl)c(CO)n1Cc1ccccc1Cl
Reaction #6577
2-n-butyl 4-chloro 1-(2-chlorophenyl)methyl-5-hydroxymethyl-1H-imidazole
Ausbeute 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
ClCc1ccc(-c2ccccn2)cc1
Reaction #7475
4-(pyridin-2-yl)benzyl chloride
Ausbeute 53.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCC1Cc2c(ccc(OC)c2Cl)C1=O
Reaction #7950
2-butyl-4-chloro-5-methoxy-1-indanone
Ausbeute 15.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2cccc(OC(C)C)c2s1
Reaction #9218
title compound
Ausbeute 25.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N(NCl)C(=O)c1ccccc1
Reaction #10412
chloro-benzoylhydrazinecarboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2cc(Br)ccc2c1Cl
Reaction #40266
6-bromo-1-chloro-2-naphthol
Ausbeute 95.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cncc2[nH]c3ccc(Cl)cc3c12
Reaction #40499
6-chloro-4-methyl-9H-β-carboline
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NC(=O)c1cc(Cl)cc([N+](=O)[O-])c1N
Reaction #40910
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(=O)c1nc(NC=O)sc1Cl
Reaction #41810
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(O)c(Cl)c(C)c1-c1cccc(C=O)c1
Reaction #43931
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1cn(C)c(=O)c(Cl)c1Cl
Reaction #44188
4,5-dichloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl ester
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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