部分構造検索

11394

COC(=O)c1ccc(CN([C@@H]2CCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7126
4-[[(1R,2S)-(2-carbamoyl-cyclohexyl)-(4-chlorobenzenesulfonyl)-amino]-methyl]-benzoic acid methyl ester
収率 22.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7136
titled compound
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7147
titled compound
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1c2cn[nH]c2/C(=N\O)[C@H](CC)N1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44006
product 63
DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(CO)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44023
mixture
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(COC(=O)N(C)C)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44024
112
収率 136.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1Cc2cn[nH]c2CC1c1ccc(Cl)cc1
Reaction #44031
benzyl 6-(4-chlorophenyl)-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)cc1)N1[C@H](CO)Cc2[nH]ncc2[C@@H]1CO
Reaction #44042
cis-(5-(4-Chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-4,6-diyl)dimethanol
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)OCC1c2cn[nH]c2CCN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44043
(5-(4-Chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-4-yl)methyl dimethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCNS(=O)(=O)c1ccc(Cl)c(C(=O)O)c1
Reaction #60949
title compound
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(S(=O)(=O)N2CCCC2)ccc1Cl
Reaction #60952
title compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNS(=O)(=O)c1ccc(N2CCCC2)c(C(=O)O)c1
Reaction #60959
title compound
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNS(=O)(=O)c1ccc(N2CCOCC2)c(C(=O)O)c1
Reaction #60967
title compound
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCS(=O)(=O)c1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157575
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1)N1CCCC1
Reaction #157633
title compound
収率 17.2%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1cc(S(=O)(=O)NC2CCC(C(=O)N3CCNCC3c3ccccc3)CC2)ccc1Cl
Reaction #175892
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(NC(=O)C(CC)NS(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #176216
DOI: 10.1039/C8SC04228D
CN1CC=C(c2cn(S(=O)(=O)c3ccc(Cl)cc3)c3ccc(F)cc23)CC1
Reaction #180466
DOI: 10.1039/C8SC04228D
COC(=O)CCCCCCNC(=O)C(COS(C)(=O)=O)NS(=O)(=O)c1ccc(Cl)cc1
Reaction #181764
DOI: 10.1039/C8SC04228D
Cc1cn(CC(=O)N2CCN(S(=O)(=O)c3c(Cl)cc(Cl)cc3[N+](=O)[O-])C(=O)C2)c(=O)[nH]c1=O
Reaction #182763
DOI: 10.1039/C8SC04228D
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