Busqueda de Subestructura

204857

Cc1nn(COCC[Si](C)(C)C)c(C)c1B1OC(C)(C)C(C)(C)O1
Reaction #185315
DOI: 10.1039/C8SC04228D
Cc1cc(-c2c(C)nn(C)c2C)cc(C)c1Br
Reaction #324805
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #324906
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C)c(C)c1B1OC(C)(C)C(C)(C)O1
Reaction #371840
DOI: 10.1039/C8SC04228D
CC(=O)OC1CSC(Oc2cccc(-c3c(C)nn(C)c3C)c2)C(OC(C)=O)C1OC(C)=O
Reaction #397061
DOI: 10.1039/C8SC04228D
Cc1nn(CC23CC4CC(CC(C4)C2)C3)c(C)c1B1OC(C)(C)C(C)(C)O1
Reaction #423755
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C)c(C)c1-c1cccc2c1CC[C@H](N(C)Cc1ccccc1)C2
Reaction #507959
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C)c(C)c1-c1cccc2c1CC[C@H](N(Cc1ccccc1)C(=O)C(C)(C)C)C2
Reaction #507962
coupling product
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cnc2ccc(-c3c(C)nn(C(=O)OC(C)(C)C)c3C)nc2c1N[C@H]1CC[C@H](CN(C)C)CC1
Reaction #613396
crude product
Rendimiento 76.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(Cc2cccc(F)c2)c(C)c1B1OC(C)(C)C(C)(C)O1
Reaction #618619
pure product
Rendimiento 94.6%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1cc(-c2cnc3c(c2)c(-c2c(C)nn(Cc4cccc(F)c4)c2C)cn3S(=O)(=O)c2ccc(C)cc2)ccc1OC
Reaction #618682
titled compound
Rendimiento 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc3c(c2)c(-c2c(C)nn(Cc4cc(F)cc(F)c4)c2C)cn3S(=O)(=O)c2ccc(C)cc2)cc1NS(C)(=O)=O
Reaction #618684
crude compound
Rendimiento 113.7%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1cc(-c2cnc3c(c2)c(-c2c(C)nn(Cc4cc(F)ccc4F)c2C)cn3S(=O)(=O)c2ccc(C)cc2)ccc1OC
Reaction #618686
titled compound
Rendimiento 61.4%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1cc(-c2cnc3c(c2)c(-c2c(C)nn(Cc4cc(F)cc(F)c4)c2C)cn3S(=O)(=O)c2ccc(C)cc2)ccc1OC
Reaction #618687
titled compound
Rendimiento 77.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc3c(-c4c(C)nn(Cc5cc(F)cc(F)c5)c4C)cn(C(=O)OC(C)(C)C)c3nc2C2CC2)cc1N(C(=O)OC(C)(C)C)S(C)(=O)=O
Reaction #618699
titled compound
Rendimiento 42.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc3c(-c4c(C)nn(Cc5cccc(F)c5)c4C)cn(C(=O)OC(C)(C)C)c3nc2C2CC2)cc1N(C(=O)OC(C)(C)C)S(C)(=O)=O
Reaction #618701
titled compound
Rendimiento 25.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc3c(c2)c(-c2c(C)nn(Cc4cccc(F)c4)c2C)cn3S(=O)(=O)c2ccc(C)cc2)c(OC)c1NS(C)(=O)=O
Reaction #618703
titled compound
Rendimiento 64.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc3c(c2)c(-c2c(C)nn(Cc4cccc(F)c4)c2C)c(C2CC2)n3C(=O)OC(C)(C)C)cc1N(C(=O)OC(C)(C)C)S(C)(=O)=O
Reaction #618705
crude product
Rendimiento 122.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3c(C)nn(Cc4cccc(F)c4)c3C)c3cc(-c4cccc(N5CCN(C(=O)OC(C)(C)C)CC5)c4)cnc32)cc1
Reaction #618716
tert-butyl 4-(3-(3-(1-(3-fluorobenzyl)-3,5-dimethyl-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)phenyl)piperazine-1-carboxylate
Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3c(C)nn(Cc4cccc(F)c4)c3C)c3cc(-c4ccc(N5CCN(C(=O)OC(C)(C)C)CC5)cc4)cnc32)cc1
Reaction #618719
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
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