Busqueda de Subestructura

420116

CC(C)(C)OC(=O)n1cc(-c2cn(Cc3ccccc3)nn2)c2cccnc21
Reaction #73853
tert-butyl 3-(1-benzyl-1H-1,2,3-triazol-4-yl)pyrrolo[2,3-b]pyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cc(-c2cn(Cc3ccc(Cl)cc3)nn2)c2cccnc21
Reaction #73855
tert-butyl 3-[1-(4-chlorobenzyl)-1H-1,2,3-triazol-4-yl]pyrrolo[2,3-b]pyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cnc3c(c2)c(-c2cn(Cc4ccccc4)nn2)cn3C(=O)OC(C)(C)C)cn1
Reaction #73857
tert-butyl 3-(1-benzyl-1H-1,2,3-triazol-4-yl)-5-(1-methyl-1H-pyrazol-4-yl)pyrrolo[2,3-b]pyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC#Cc1cn(C(=O)OC(C)(C)C)c2nccc(Oc3ccc([N+](=O)[O-])cc3F)c12
Reaction #376819
DOI: 10.1039/C8SC04228D
CN(C)CC#Cc1cn(C(=O)OC(C)(C)C)c2nccc(Oc3ccc([N+](=O)[O-])cc3F)c12
Reaction #434735
desired product
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cc(-c2cnn(Cc3cccc([N+](=O)[O-])c3)c2)c2cc(-c3cccc(NS(C)(=O)=O)c3)cnc21
Reaction #618662
pure product
Rendimiento 68.0%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)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
Cc1nn(Cc2cccc(F)c2)c(C)c1-c1cn(C(=O)OC(C)(C)C)c2ncc(-c3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)c(NS(C)(=O)=O)c3)cc12
Reaction #618753
titled compound
Rendimiento 2.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(Cc2cc(F)cc(F)c2)c(C)c1-c1cn(C(=O)OC(C)(C)C)c2nc(C3CC3)c(-c3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)cc3)cc12
Reaction #618756
titled compound
Rendimiento 45.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(Cc2cccc(F)c2)c(C)c1-c1c(C2CC2)n(C(=O)OC(C)(C)C)c2ncc(-c3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)cc3)cc12
Reaction #618761
crude product
Rendimiento 178.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cnc3c(c2)c(-c2c(C)nn(Cc4cccc(F)c4)c2C)cn3C(=O)OC(C)(C)C)cc1NS(C)(=O)=O
Reaction #618767
titled compound
Rendimiento 63.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc3c(c2)c(-c2cnn(Cc4cccnc4)c2)cn3C(=O)OC(C)(C)C)cc1N(C(=O)OC(C)(C)C)S(C)(=O)=O
Reaction #618778
titled compound
Rendimiento 38.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(Cc2cc(F)cc(F)c2)c(C)c1-c1cn(C(=O)OC(C)(C)C)c2ncc(-c3ccc(F)c(N(C(=O)OC(C)(C)C)S(C)(=O)=O)c3)cc12
Reaction #618795
crude compound
Rendimiento 91.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(Cc2cccc(F)c2)c(C)c1-c1cn(C(=O)OC(C)(C)C)c2ncc(-c3ccc(N(C(=O)OC(C)(C)C)C4CCN(C(=O)OC(C)(C)C)CC4)cc3)cc12
Reaction #618849
titled compound
Rendimiento 25.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(-c3cnc4c(c3)c(-c3cnn(Cc5cccc(F)c5)c3)cn4C(=O)OC(C)(C)C)cc2NS(C)(=O)=O)CC1
Reaction #618864
titled compound
Rendimiento 18.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(-c3cnc4c(c3)c(-c3cnn(CCc5ccccc5)c3)cn4C(=O)OC(C)(C)C)cc2NS(C)(=O)=O)CC1
Reaction #618866
titled compound
Rendimiento 15.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2c[nH]c3ncccc23)c2ccccc2n1
Reaction #962227
4-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolin-2-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccc3c(-c4c[nH]c5ncccc45)ccnc3n2)cc1
Reaction #962228
2-phenyl-5-(1H-pyrrolo[2,3-b]pyridin-3-yl)-1,8-naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1
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