反応 #62307

ord-01a90d08fb0a473ea7da21d086405516

反応方程式

Nc1cc(F)c2[nH]nc(/C=C/c3cccnc3)c2c1
7-fluoro-3-[(E)-2-(pyridin-3-yl)-vinyl]-1H-indazol-5-ylamine
O=C(O)c1ccco1
2-furancarboxylic acid
O=C(Nc1cc(F)c2c(c1)c(/C=C/c1cccnc1)nn2C(=O)c1ccco1)c1ccco1
title compound
収率 37.9%
O=C(Nc1cc(F)c2c(c1)c(/C=C/c1cccnc1)nn2C(=O)c1ccco1)c1ccco1
Furan-2-carboxylic acid{7-fluoro-1-(furan-2-carbonyl)-3-[(E)-2-(pyridin-3-yl)-vinyl]-1H-indazole-5-yl}-amide
収率 37.9%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他with the method of Example 127, purification by LC-MS

実験手順

Following amidation using 217 mg of 7-fluoro-3-[(E)-2-(pyridin-3-yl)-vinyl]-1H-indazol-5-ylamine and 286 mg of 2-furancarboxylic acid in accordance with the method of Example 127, purification by LC-MS was carried out, to afford 143 mg of the title compound as yellow crystals.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07429609B2uspto-grants-2008_09