بحث البنية الفرعية

Fc1ccc(S)c(F)c1

Cl.O=S(=O)(c1ccc(F)cc1F)n1ccc2c(N3CCNCC3)cccc21
Reaction #8417
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(CN1CC(CS(=O)(=O)c2ccc(F)cc2F)C1)c1ccc(F)cc1
Reaction #10302
2-(3-{[(2,4-difluorophenyl)sulfonyl]methyl}azetidin-1-yl)-1-(4-fluorophenyl)ethanone hydrochloride
المردود 13.6%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(Sc2ccc(F)cc2Br)c(F)c1
Reaction #43499
1-Bromo-2-(2,4-difluoro-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@H](OCCCCBr)CC1)S(=O)(=O)c1ccc(F)cc1F
Reaction #53834
trans-N-[4-(4-Bromo-butoxy)-cyclohexyl]-2,4-difluoro-N-methyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc(N2CCOCC2)c(C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)c1F
Reaction #61030
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(Br)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #67106
desired material
المردود 5.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #67107
title compound
المردود 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4C[C@@H](C)O[C@@H](C)C4)o3)c3cnn(S(=O)(=O)c4ccccc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #67113
title compound
المردود 80.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4C[C@@H](C)O[C@@H](C)C4)o3)c3cn[nH]c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #67150
title compound
المردود 7.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4C[C@@H](C)N(C(C)C)[C@@H](C)C4)o3)c3cn[nH]c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #67164
title compound
المردود 2.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4CCN5CCC[C@H]5C4)o3)c3cn[nH]c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #67168
title compound
المردود 3.5%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ncc(Cl)s1)c1cc(Cl)c(Oc2ccc(Cl)cc2C2CNC2)cc1F
Reaction #74513
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ncns3)cc2F)ccn1
Reaction #74516
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(c2ncns2)S(=O)(=O)c2cc(Cl)c(Oc3ccc(Cl)cc3C3CCN(C(=O)OC(C)(C)C)CC3)cc2F)c(OC)c1
Reaction #74523
tert-butyl 4-[5-chloro-2-(2-chloro-4-{[(2,4-dimethoxybenzyl)(1,2,4-thiadiazol-5-yl)amino]sulfonyl}-5-fluorophenoxy)phenyl]piperidine-1-carboxylate
المردود 97.6%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc(F)cn1)c1cc(Cl)c(Oc2ccc(C(F)(F)F)cc2C2CCNCC2)cc1F
Reaction #74527
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1[nH]ncc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2nncs2)cc1Cl
Reaction #74529
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ncns1)c1cc(F)c(Oc2ccc(C(F)(F)F)cc2-c2ccnnc2)cc1F
Reaction #74531
2,5-difluoro-4-[2-pyridazin-4-yl-4-(trifluoromethyl)phenoxy]-N-1,2,4-thiadiazol-5-ylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ccncn3)cc2Cl)ccn1
Reaction #74535
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nccc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2ccncn2)cc1Cl
Reaction #74536
desired product
المردود 27.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3nncs3)cc2Cl)ccn1
Reaction #74537
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي