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Cc1ccc(S)c(Cl)c1

CS(=O)c1ccc(-c2cc(Cl)ccc2OCC(=O)O)cc1Cl
Reaction #44351
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2oncc2C(=O)C2CC2)cc1Cl
Reaction #49724
4-cyclopropylcarbonyl-5-[3-chloro-4-(methylsulphonyl)phenyl]isoxazole
DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cc1cc(Cl)c(Sc2ccc(O)c(Cc3ccc(=O)[nH]c3)c2)c(Cl)c1)C(=O)O
Reaction #63568
4-(4'-Hydroxy-3'-(6-oxo-3(1H)-pyridylmethyl) phenylthio)-3,5-dichlorophenylalanine
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(S(N)(=O)=O)ccc1CNc1nc(NC2(C(F)(F)F)CC2)c2nc(-c3ccc(F)cc3)ccc2n1
Reaction #70608
4-{[6-(4-Fluoro-phenyl)-4-(1-trifluoromethyl-cyclopropylamino)-pyrido[3,2-d]pyrimidin-2-ylamino]-methyl}-3-methyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1cc2c(cc1Cl)CCC2=O
Reaction #94210
5-Chloro-6-sulfamoyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1cc2c(cc1Cl)CC(Br)C2=O
Reaction #94211
2-Bromo-5-chloro-6-sulfamoyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCNS(=O)(=O)c1cc2c(cc1Cl)CCC2=O
Reaction #94212
5-Chloro-6-n-propylsulfamoyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCNS(=O)(=O)c1cc2c(cc1Cl)CC(Br)C2=O
Reaction #94213
2-Bromo-5-chloro-6-n-propylsulfamoyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCc2cc(Cl)c(S(=O)(=O)NCc3ccccc3)cc21
Reaction #94214
6-benzylsulfamoyl-5-chloro-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc(Cl)c(S(N)(=O)=O)cc2C1=O
Reaction #94218
raw product
DOI: 10.6084/m9.figshare.5104873.v1
CC1(Br)Cc2cc(Cl)c(S(N)(=O)=O)cc2C1=O
Reaction #94219
2-bromo-5-chloro-2-methyl-6-sulfamoyl-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(/C(=N/OC2CCCC2)c2ccc(S(C)(=O)=O)c(Cl)c2)[nH]c1=O
Reaction #157879
(E)-6-{[3-chloro-4-(methylsulfonyl)phenyl](cyclopentyloxyimino)methyl}-3-methylpyridin-2(1H)-one
المردود 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)NCc2ccc3c(ccn3C)c2)c(Cl)c1
Reaction #160251
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)N(Cc2ccc3c(ccn3C)c2)c2ncc(Cl)cc2Cl)c(Cl)c1
Reaction #160253
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)NCc2ccc3c(cnn3CC)c2)c(Cl)c1
Reaction #160264
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)N(Cc2ccc3c(cnn3CC)c2)c2ncc(C(F)(F)F)cc2Cl)c(Cl)c1
Reaction #160265
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(S(=O)(=O)N(Cc2ccc3c(cnn3C)c2)c2ncc(C(F)(F)F)cc2Cl)c(Cl)c1
Reaction #160284
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)N(Cc2ccc3c(cnn3C3CC3)c2)c2ncc(C(F)(F)F)cc2Cl)c(Cl)c1
Reaction #160295
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)N(Cc2ccc3c(cnn3C3CC3)c2)c2ncc(Cl)cc2Cl)c(Cl)c1
Reaction #160296
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)NCc2cnc3c(ccn3C)c2)c(Cl)c1
Reaction #160300
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي