بحث البنية الفرعية

68546

Cc1ccc2nc(-c3ccc(NC(=O)c4ccccc4)cc3)sc2c1
Reaction #426723
title compound
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(NC(=O)c4ccc([N+](=O)[O-])cc4)cc3)sc2c1
Reaction #426724
title compound
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(NC(=O)c4ccccc4N)cc3)sc2c1
Reaction #426725
title compound
المردود 14.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(NC(=O)c4cccc(N(C)C)c4)cc3)sc2c1
Reaction #426726
title compound
المردود 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(NC(=O)c4ccc(N(C)C)cc4)cc3)sc2c1
Reaction #426727
title compound
المردود 7.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1cccc(C(=O)Nc2ccc(-c3nc4ccc(C)cc4s3)cc2)c1
Reaction #426728
title compound
المردود 18.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(N)c(OS(=O)(=O)C(F)(F)F)c3)sc2c1
Reaction #450489
2-(4-Amino-3-trifluoromethylsulphonyloxyphenyl)-6-methylbenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)Nc2ccc(-c3nc4ccc(C)cc4s3)cc2)cc1
Reaction #944256
N-[4-(6-methylbenzothiazol-2-yl)phenyl]-4-methylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COC1(c2nc3ccc(C)cc3s2)C=CC(=NS(=O)(=O)c2ccc(C)cc2)C=C1
Reaction #944257
title compound
المردود 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](OC(C)(C)C)c1c(C)cc2nc(-c3ccc([N+](=O)[O-])c(F)c3)sc2c1-c1ccc(Cl)cc1
Reaction #966577
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](OC(C)(C)C)c1c(C)cc2nc(-c3ccc(NC)c([N+](=O)[O-])c3)sc2c1-c1ccc(Cl)cc1
Reaction #966607
(S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(4-(methylamino)-3-nitrophenyl)benzo[d]thiazol-6-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](OC(C)(C)C)c1c(C)cc2nc(-c3ccc(NC)c(N)c3)sc2c1-c1ccc(Cl)cc1
Reaction #966608
(S)-ethyl 2-(2-(3-amino-4-(methylamino)phenyl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2nc(-c3ccc4c(c3)CC(=O)N4)sc2c(-c2ccc(Cl)cc2)c1[C@H](OC(C)(C)C)C(=O)O
Reaction #966644
(S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-oxoindolin-5-yl)benzo[d]thiazol-6-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2nc(-c3ccc4c(c3)CC(=O)N4C)sc2c(-c2ccc(Cl)cc2)c1[C@H](OC(C)(C)C)C(=O)O
Reaction #966647
(S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(1-methyl-2-oxoindolin-5-yl)benzo[d]thiazol-6-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](OC(C)(C)C)c1c(C)cc2nc(-c3ccc4c(c3)C(C)(C)C(=O)N4C)sc2c1-c1ccc(Cl)cc1
Reaction #966662
(S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(1,3,3-trimethyl-2-oxoindolin-5-yl)benzo[d]thiazol-6-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2nc(-c3ccc4c(c3)C(C)(C)C(=O)N4C)sc2c(-c2ccc(Cl)cc2)c1[C@H](OC(C)(C)C)C(=O)O
Reaction #966663
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)Nc2ccc(-c3nc4ccc(C)cc4s3)cc2)cc1
Reaction #1037301
DOI: 10.1039/C8SC04228D
Cc1ccc2nc(-c3ccc(NC(=O)c4ccco4)cc3)sc2c1
Reaction #1148896
expected product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(NC(=O)c4ccco4)cc3)sc2c1
Reaction #1148897
desired compound
المردود 46.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(NC(=O)N4CCN(c5ccnc6cc(Cl)ccc56)CC4)cc3)sc2c1
Reaction #1440568
title product
DOI: 10.6084/m9.figshare.5104873.v1
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