Teilstruktursuche

1226199

C[C@]1(CS(=O)(=O)N2CCC(c3ccc(F)cc3)CC2)NC(=O)NC1=O
Reaction #60664
(5S)-5-({[4-(4-fluorophenyl)piperidin-1-yl]sulfonyl}methyl)-5-methylimidazolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)N(CC2(CS(=O)(=O)N3CCC(Oc4ccc(Cl)cn4)CC3)NC(=O)NC2=O)C(=O)C1(C)C
Reaction #60671
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(CCOCc2ccccc2)(CS(=O)(=O)N2CCC(Oc3ccc(Cl)cn3)CC2)N1
Reaction #60673
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)c2ccccc2C1=O.O=[SH](=O)Nc1ccccc1
Reaction #69034
title compound
Ausbeute 72.5%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)CCN1C(=O)c2ccccc2C1=O
Reaction #69035
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCS(=O)(=O)N1CCOCC1
Reaction #69036
2-(2-(morpholinosulfonyl)ethyl)isoindole-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)c2ccccc2C1=O.O=[SH](=O)Nc1ccc(I)cc1
Reaction #69037
2-phthalimidoethane N-(4-iodophenyl)sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)c2ccccc2C1=O.CN[SH](=O)=O
Reaction #69039
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)c2ccccc2C1=O.CN(C)[SH](=O)=O
Reaction #69040
2-phthalimidoethane N,N-dimethylsulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)Cn1nnnc1S
Reaction #173580
DOI: 10.1039/C8SC04228D
NS(=O)(=O)Cn1nnnc1S
Reaction #198434
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(CCOCc2ccccc2)(CS(=O)(=O)N2CCC(Oc3ccc(Cl)cn3)CC2)N1
Reaction #206278
DOI: 10.1039/C8SC04228D
Cc1ccc(NC(=O)Nc2nc(CNS(=O)(=O)CCN)cs2)c(C(=O)C2CCCC2)c1
Reaction #219051
2-Amino-ethanesulfonic acid {2-[3-(2-cyclopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazol-4-ylmethyl}-amide
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNS(=O)(=O)C1CCN(C(=O)OCc2ccccc2)C1
Reaction #237298
DOI: 10.1039/C8SC04228D
CC1(CS(=O)(=O)N2CCc3cc(-c4cnc(C5CC5)nc4)ncc3C2)NC(=O)NC1=O
Reaction #242346
DOI: 10.1039/C8SC04228D
CC1(CS(=O)(=O)N2CCc3cc(-c4ccc(C5CC5)nc4)ncc3C2)NC(=O)NC1=O
Reaction #255049
DOI: 10.1039/C8SC04228D
O=C1c2c(c(OS(=O)(=O)CCN3C(=O)c4ccccc4C3=O)c3cccnc3c2OC(c2ccccc2)c2ccccc2)CN1Cc1ccc(F)cc1
Reaction #261343
DOI: 10.1039/C8SC04228D
CC(C)Nc1cccnc1N(C)C1CCN(C(=O)c2cc3cc(NS(=O)(=O)CCN4C(=O)c5ccccc5C4=O)ccc3[nH]2)CC1
Reaction #281311
DOI: 10.1039/C8SC04228D
O=C(NC(CS(=O)(=O)N1CCOCC1)C(=O)OCc1ccccc1)OCc1ccccc1
Reaction #285186
DOI: 10.1039/C8SC04228D
Cn1c(-c2cncc(CNS(=O)(=O)CCN3C(=O)c4ccccc4C3=O)c2)c(C#N)c2ccc(Cl)cc21
Reaction #288912
DOI: 10.1039/C8SC04228D
Seite 1Weiter