反応 #71356

ord-cb48339784fb41b5b6cdbf7ed92c34d3

反応方程式

CN1CCN(c2ccc(N)cc2)CC1
4-(4-methylpiperazin-1-yl)-aniline
O=C(O)c1ccc(-c2cccc3ccccc23)c2nccnc12
8-naphthalen-1-yl-quinoxaline-5-carboxylic acid
OB(O)c1cccc2ccccc12
1-naphtylboronic acid
CN1CCN(c2ccc(NC(=O)c3ccc(-c4cccc5ccccc45)c4nccnc34)cc2)CC1
Title compound
CN1CCN(c2ccc(NC(=O)c3ccc(-c4cccc5ccccc45)c4nccnc34)cc2)CC1
8-Naphthalen-1-yl-quinoxaline-5-carboxylic acid [4-(4-methyl-piperazin-1-yl)-phenyl]-amide

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The title compound was prepared in analogy to the procedure
  2. 2
    その他The latter compound was synthesized

実験手順

The title compound was prepared in analogy to the procedure described in in Step 14.1 but stirring the reaction mixture overnight and using 4-(4-methylpiperazin-1-yl)-aniline (WO2006000420) and 8-naphthalen-1-yl-quinoxaline-5-carboxylic acid. The latter compound was synthesized as described in Steps 1.2-1.7 but using 1-naphtylboronic acid in Step 1.4. Title compound: ESI-MS: 474.0 [M+H]+; tR=4.34 min (System 1); TLC: Rf=0.45 (DCM/MeOH/NH3aq, 94:5:1).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08536175B2uspto-grants-2013_09