Участвует в 432 реакциях

492

CS(=O)(=O)c1ccc(Nc2cncc(Cl)n2)cc1
Reaction #390
Выход 22.0%750 AstraZeneca ELN dataset
NC(=O)c1ccc2ncn(-c3cncc(Cl)n3)c2c1
Reaction #44412
1-(6-chloropyrazin-2-yl)-1H-benzimidazole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@H](c1ccccc1)N(C)c1cncc(Cl)n1
Reaction #44414
desired product
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](Nc1cncc(Cl)n1)c1ccc(F)c(F)c1
Reaction #44420
pyrazine
Выход 35.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(Nc1ccc(Sc2cncc(Cl)n2)cc1)C1CC1
Reaction #44474
title compound
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccccc1Oc1cncc(Cl)n1
Reaction #44554
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1cccc(Oc2cncc(Cl)n2)c1
Reaction #44555
title compound
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1ccc(Oc2cncc(Cl)n2)c2ccccc12
Reaction #44556
title compound
Выход 68.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cncc(Oc2ccccc2Cl)n1
Reaction #44557
title compound
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cccc(Oc2cncc(Cl)n2)c1
Reaction #44558
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cncc(Oc2ccccc2-c2ccccc2)n1
Reaction #44559
title compound
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cncc(Oc2cccc(-c3ccccc3)c2)n1
Reaction #44560
title compound
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cncc(Oc2ccc(-c3ccccc3)cc2)n1
Reaction #44561
title compound
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1cccc(Oc2cncc(Cl)n2)c1
Reaction #44562
title compound
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1ccc(Oc2cncc(Cl)n2)cc1
Reaction #44563
title compound
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CCc2c(Oc3cncc(Cl)n3)cccc21
Reaction #44564
title compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CCc2cc(Oc3cncc(Cl)n3)ccc21
Reaction #44565
title compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CCc2ccc(Oc3cncc(Cl)n3)cc21
Reaction #44566
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CCc2cccc(Oc3cncc(Cl)n3)c21
Reaction #44567
title compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cncc(Oc2ccnc3ccccc23)n1
Reaction #44568
title compound
Выход 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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