反応 #45515

ord-93104affc175448093ce0a1d0b874d0a

反応方程式

COc1cc(-c2csc3c(N)cnc(N=CN(C)C)c23)ccc1NC(=O)c1cc2ccccc2n1C
N-[4-(7-amino-4-{[(dimethylamino)methylene]amino}thieno[3,2-c]pyridin-3-yl)-2-methoxyphenyl]-1-methyl-1H-indole-2-carboxamide
O=S(=O)(Cl)c1ccccc1
phenylsulfonyl chloride
COc1cc(-c2csc3c(NS(=O)(=O)c4ccccc4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
title compound
COc1cc(-c2csc3c(NS(=O)(=O)c4ccccc4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
N-(4-{4-amino-7-[(phenylsulfonyl)amino]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

The title compound was prepared using N-[4-(7-amino-4-{[(dimethylamino)methylene]amino}thieno[3,2-c]pyridin-3-yl)-2-methoxyphenyl]-1-methyl-1H-indole-2-carboxamide and phenylsulfonyl chloride using General Procedure G followed by General Procedure M. 1H NMR (DMSO-d6, 400 MHz) δ 9.80 (br, 1H), 9.49 (s, 1H), 7.97 (d, 1H), 7.75 (d, 2H), 7.70 (d, 1H), 7.64 (d, 1H), 7.58 (m, 3H), 7.51 (s, 1H), 7.34 (m, 2H), 7.17 (m, 2H), 7.15 (s, 1H), 7.05 (d, 1H), 5.50 (br, 2H), 4.03 (s, 3H), 3.90 (s, 3H); MS: (MH)+ 584.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07737160B2uspto-grants-2010_06