Recherche de Sous-structure

1251169

COC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cncc2ccccc12
Reaction #45362
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2cccc(NC(=O)c3ccc(-c4cncc5ccccc45)c4nccnc34)c2)CC1
Reaction #71360
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(N)=O)N1CCN(Cc2cc3nc(-c4cnc(N)c5cc(F)ccc45)nc(N4CCOCC4)c3s2)CC1
Reaction #183978
DOI: 10.1039/C8SC04228D
Cn1c(CN2CCN(C(C)(C)C)CC2)nc2c(N3CCOCC3)nc(-c3cnc(N)c4ccccc34)nc21
Reaction #210304
DOI: 10.1039/C8SC04228D
CC(C)(O)c1cc2nc(-c3cnc(N)c4ccccc34)nc(N3CCOCC3)c2s1
Reaction #238899
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1ccc(-c2cncc3ccccc23)cc1[N+](=O)[O-]
Reaction #259694
DOI: 10.1039/C8SC04228D
CC(C)(C(N)=O)N1CCN(Cc2cc3nc(-c4cnc(N)c5ccc(F)cc45)nc(N4CCOCC4)c3s2)CC1
Reaction #274221
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1ccc(-c2cncc3ccccc23)cc1Nc1ccc(F)cc1
Reaction #289533
DOI: 10.1039/C8SC04228D
COC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cncc2ccccc12
Reaction #304709
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(CN2CCC(N3CCOCC3)CC2)nc2c(N3CCOCC3)nc(-c3cnc(N)c4ccccc34)nc21
Reaction #384580
DOI: 10.1039/C8SC04228D
—
Reaction #489279
hydrochloride salt
Rendement 98.8%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(-c2cncc3ccccc23)cc2cn[nH]c12
Reaction #489314
4-(7-chloro-1H-indazol-5-yl)-isoquinoline
Rendement 72.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1ccc(-c2cncc3ccccc23)cc1[N+](=O)[O-]
Reaction #541694
tert-butyl 4-(isoquinolin-4-yl)-2-nitrobenzoate
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccc3c(=O)n(C)cc(-c4cc(S(C)(=O)=O)ccc4OCC4CC4)c3c2)cn1
Reaction #605463
title compound
Rendement 34.9%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)c1ccc(OC)c(-c2cn(C)c(=O)c3ccc(-c4cnn(C)c4)cc23)c1
Reaction #605484
title compound
Rendement 55.7%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1cc(-c2cn(C)c(=O)c3ccc(-c4cnn(C)c4)cc23)c(OC)cc1F
Reaction #605488
title compound
Rendement 26.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(CS(C)(=O)=O)cc1-c1cn(C)c(=O)c2ccc(-c3cnn(C)c3)cc12
Reaction #605495
title compound
Rendement 19.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc(S(C)(=O)=O)ccc2OCC2CC2)c2ccccc2c1=O
Reaction #605496
title compound
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2nc(CS(C)(=O)=O)ncc2OCC2CC2)c2ccccc2c1=O
Reaction #605536
title compound
Rendement 42.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccc3c(=O)n(C)cc(-c4nc(CS(C)(=O)=O)ncc4OCC4CC4)c3c2)cn1
Reaction #605538
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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