Busqueda de Subestructura

Cl.OC1CNC1

COc1cc(OC2CNC2)ccc1Nc1ncc(Cl)c(-c2cnc3ccccn23)n1
Reaction #160
Rendimiento 0.0%
OC1CN(CCCOCCc2ccc3ccsc3c2)C1
Reaction #7534
1-{3-[2-(1-benzothiophen-6-yl)ethoxy]propyl}-3-azetidinol
Rendimiento 24.5%DOI: 10.6084/m9.figshare.5104873.v1
OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7536
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol
Rendimiento 64.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(N3CC(O)C3)nc2c1C#N
Reaction #45696
7-Fluoro-2-(3-hydroxyazetidin-1-yl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H](c2ccc(Cl)cc2)N2CC(=O)C2)cc1
Reaction #46334
1-{(R*)-(4-chlorophenyl)[4-(methoxycarbonyl)phenyl]methyl}azetidin-3-one
Rendimiento 83.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H](c2ccc(Cl)cc2)N2CC(O)C2)cc1
Reaction #46335
1-{(R*)-(4-chlorophenyl)[4-(methoxycarbonyl)-phenyl]methyl}azetidin-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
COC1CN(C(=O)c2cccc3c2nc(C(=O)NC2CCN(C(C)C)CC2)n3Cc2cc(-c3ccc(Cl)s3)on2)C1
Reaction #46840
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(NC(=O)c2nc3c(C(=O)N4CC(O)C4)cccc3n2CCc2ccc(Cl)cc2)CC1
Reaction #46844
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1CN(C(=O)c2cccc3c2nc(C(=O)NC2CCN(C(C)C)CC2)n3CCc2ccc(Cl)cc2)C1
Reaction #46845
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1c(-c2cccnc2)c[nH]n1-c1cc(N2CC(O)C2)ncn1
Reaction #66187
2-[6-(3-Hydroxyazetidin-1-yl)pyrimidin-4-yl]-4-pyridin-3-yl-1,2-dihydro-3H-pyrazol-3-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #91824
solid
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)ccc3F)nc12)N1CC(O)C1
Reaction #92253
final product
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cnn2ccc(N3CC(F)(F)C[C@@H]3c3cccc(F)c3)nc12)N1CC(O)C1
Reaction #92266
final product
Rendimiento 48.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)ccc3Cl)nc12)N1CC(O)C1
Reaction #92267
final product
Rendimiento 85.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccc(F)c2)CCCN1c1ccn2ncc(NC(=O)N3CC(O)C3)c2n1
Reaction #92272
final product
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)cc(Cl)c3)nc12)N1CC(O)C1
Reaction #92273
final product
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)ccc3C(F)F)nc12)N1CC(O)C1
Reaction #92274
final product
DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CN(C(=O)Nc2cnn3ccc(N4CCC[C@@H]4c4cc(F)ccc4Cl)nc23)C1
Reaction #92281
final product
Rendimiento 71.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cccc(F)c3)nc12)N1CC(O)C1
Reaction #92286
final product
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cnc1N1CC(O)C1
Reaction #159610
title compound ( D62 )
DOI: 10.6084/m9.figshare.5104873.v1
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