بحث البنية الفرعية

1428196

Cl
Reaction #249088
DOI: 10.1039/C8SC04228D
O=C(O)/C=C\C(=O)O.O=S(=O)(c1ccc(Cl)cc1)C1CCN(Cc2ccccc2)C1
Reaction #323263
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1ccc(Cl)cc1)C1CCNC1
Reaction #323269
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)C2CCNC2)cc1.Cl
Reaction #323271
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)N1CCC(S(=O)(=O)c2ccc(Cl)cc2)C1
Reaction #323291
white crystals
المردود 46.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNC(=O)N1CCC(S(=O)(=O)c2ccc(Cl)cc2)C1
Reaction #323292
white crystals
المردود 51.4%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)cc1)C1CCN(Cc2ccccc2)C1
Reaction #910351
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1CC(S(=O)(=O)c2ccc(Cl)cc2)C(c2ccccc2F)N1C(=O)CNC(=O)Nc1cccc(CC(=O)O)c1
Reaction #949032
(2RS,4SR,5RS)-3-(3-{2-[2-tert-butoxycarbonyl-5-(2-fluorophenyl)-4-(4-chlorophenyl)sulphonyl-1-pyrrolidinyl]-2-oxoethyl}ureido)phenylacetic acid
المردود 38.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1(C(N)=O)CC(S(=O)(=O)c2ccc(Cl)cc2)C(c2ccccc2F)N1C(=O)CNC(=O)Nc1cccc(CC(=O)O)c1
Reaction #949039
3-(3-{2-[4-(4-chlorophenyl)sulphonyl-5-(2-fluorophenyl)-2-isobutyl carbamoyl-1-pyrrolidinyl]-2-oxoethyl}ureido)phenylacetic acid
المردود 100.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](NC(=O)[C@@H]1C[C@@H](S(=O)(=O)c2ccc(Cl)cc2Cl)CN1C(=O)C1(c2ccc(Cl)cc2)CC1)C(=O)C(=O)NC1CC1
Reaction #1112525
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(N2CCC(C)(S(=O)(=O)c3ccc(Cl)cc3)C2=O)no1
Reaction #1653417
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(N2CCC(C)(S(=O)(=O)c3ccc(Cl)cc3)C2=O)no1
Reaction #2012044
product
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)/C=C\C(=O)O.O=S(=O)(c1ccc(Cl)cc1)C1CCN(Cc2ccccc2)C1
Reaction #2068958
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1ccc(Cl)cc1)C1CCNC1
Reaction #2068967
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)C2CCNC2)cc1.Cl
Reaction #2068969
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)N1CCC(S(=O)(=O)c2ccc(Cl)cc2)C1
Reaction #2068989
white crystals
المردود 46.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNC(=O)N1CCC(S(=O)(=O)c2ccc(Cl)cc2)C1
Reaction #2068990
white crystals
المردود 51.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC(S(=O)(=O)c2ccc(Cl)cc2)C(c2ccccc2F)N1C(=O)CNC(=O)Nc1cccc(CC(=O)O)c1
Reaction #2400383
DOI: 10.1039/C8SC04228D
Reaction #2490375
solid
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(NC(=O)[C@@H]2C[C@@H](S(=O)(=O)c3ccc(Cl)cc3)CN2C(=O)C2(N3CCCCC3)CC2)CC1
Reaction #2490397
(2S,4R)-4-(4-chlorophenylsulfonyl)-N-(1-cyanocyclopropyl)-1-(1-(piperidin-1-yl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1