Recherche de Sous-structure

19445

CCCCN1CCC(CNC(=O)c2cc(Cl)cc3nc(C)oc23)CC1
Reaction #1715
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7868
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nc3cc(Cl)ccc3o2)ccc1-c1ccccn1.Cl
Reaction #7869
5-chloro-2-(3-methoxy-4-pyridin-2-yl phenyl)-1,3-benzoxazole hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(Cl)c(N)cc2o1
Reaction #9961
6-Amino-5-Chloro-2-Methylbenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(Cl)c(N)c(Cl)c2o1
Reaction #9962
6-Amino-5,7-Dichloro-2-Methylbenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Cl)cc([N+](=O)[O-])c2o1
Reaction #58138
5-chloro-7-nitro-2(3H)-benzoxazolone
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc2[nH]c(=O)oc12
Reaction #58139
7-amino-2(3H)-benzoxazolone
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c(-c2ccc(F)cc2)s1
Reaction #89191
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN[C@@H]1CNc1nc2cc(Cl)ccc2o1
Reaction #89217
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccnc(C)n2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89218
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2cncn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89220
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2cnc(C)n2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89221
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nccs2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89222
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccnc2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89224
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89225
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2ccnc2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89227
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cncs2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89228
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nccc(C)n2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89230
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccnn2C)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89232
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccnc(C)c2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(Cl)ccc3o2)c1
Reaction #89234
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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