部分構造検索

1633

COC(=O)c1ccc([N+](=O)[O-])cc1S(=O)(=O)Cl
Reaction #1092
2-Methoxycarbonyl-5-nitrobenzenesulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(S(=O)(=O)Cl)c(C)cc1N=Nc1c(C#N)[nH]n(-c2ccccc2C)c1=O
Reaction #4347
4-(4-chlorosulfonyl-2,5-dimethylphenylazo)-3-cyano-1-(2-methylphenyl)-5-pyrazolone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1ccc(C(O)(C(F)(F)F)C(F)(F)F)cc1S(=O)(=O)Cl
Reaction #4842
2-chlorosulfonyl-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzenepropanoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1ccc(C(O)(C(F)(F)F)C(F)(F)F)cc1S
Reaction #4843
2-mercapto-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzenepropanoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(S(=O)(=O)Cl)cc1-c1nc2c(C3CCCC3)nc(C)n2c(=O)[nH]1
Reaction #8718
4-Ethoxy-3-(8-cyclopentyl-6-methyl-4-oxo-3,4-dihydro-imidazol[1,5-a][1,3,5]-triazin-2-yl)-benzenesulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Nc1nc2ccc(S(=O)(=O)Cl)cc2[nH]1
Reaction #8941
desired compound
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Nc1nc2ccc(S(=O)(=O)Cl)cc2[nH]1
Reaction #11348
5-chlorosulfonyl-2-carbomethoxyamino-benzimidazole
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)c2c1cccc2S(=O)(=O)Cl
Reaction #43889
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(-c2ccc(S(=O)(=O)Cl)cc2)n1)C1(c2ccc3c(c2)OCO3)CC1
Reaction #46235
4-(6-(1-(Benzo[d][1,3]dioxol-5-yl)cyclopropane-carboxamido)pyridin-2-yl)benzene-1-sulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN1S(=O)(=O)c1ccc(-c2cccc(NC(=O)C3(c4ccc5c(c4)OCO5)CC3)n2)cc1
Reaction #46236
1-(Benzo[d][1,3]dioxol-5-yl)-N-(6-(4-(2-methylpyrrolidin-1-ylsulfonyl)phenyl)pyridin-2-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1Cc2cc(S(=O)(=O)Cl)ccc2C(C)(C)C1
Reaction #51096
title compound ( D3 )
収率 27.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1Cc2cc(S(=O)(=O)n3ccc4ccc(Cl)cc43)ccc2C(C)(C)C1
Reaction #51097
title compound ( D4 )
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(Cl)c1ccc(Oc2ccncc2)cc1
Reaction #51446
4-[(pyrid-4-yl)oxy]benzenesulfonyl chloride hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(Cl)c1ccc(Oc2ccncc2)cc1
Reaction #51450
4-((pyrid-4-yl)oxy)benzenesulfonyl chloride hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(N=Nc1cc(S(=O)(=O)Cl)ccc1OC(=O)c1ccccc1)=C(OC(=O)c1ccccc1)c1ccccc1
Reaction #54399
α-(2-Benzoyloxy-5-chlorosulfonylphenylazo)-β-benzoyloxycinnamonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Nc1nc2cc(S(=O)(=O)N(C[C@@H](O)[C@H](Cc3ccccc3)NC(=O)ONC(=O)[C@H](CC(N)=O)NC(=O)c3ccc4ccccc4n3)OC3CCCC3)ccc2[nH]1
Reaction #57454
desired product
収率 17.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Nc1nc2ccc(S(=O)(=O)NC(OC3CCCC3)[C@H](O)[C@H](Cc3ccccc3)NC(=O)OC(C)(C)C)cc2[nH]1
Reaction #57470
tert-Butyl-N-((1S,2R)-1-benzyl-3-(cyclopentyloxy)(2-[(methoxycarbonyl)amino]benzimidazol-5-ylsulfonyl)amino-2-hydroxypropyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](NS(=O)(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1)C(=O)O
Reaction #57592
N-[(4′-nitro-1,1′-biphenyl-4-yl)sulfonyl]-D-valine
収率 92.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1S(=O)(=O)Cl)CCCC2
Reaction #63677
3-Chlorosulfonyl-5,6,7,8-tetrahydro-2-naphthol methyl ether
DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc(NS(=O)(=O)C(F)(F)F)cc1
Reaction #63772
N-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamide
収率 44.1%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ