戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 448825作成日:2026年10月27日

Triethylamine → N-[6-(Dimethylamino)pyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/448825

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Diethyl cyanophosphonateHCID 76257—
反応物N2,N2-dimethylpyridine-2,5-diamineHCID 78642—
反応物5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acidHCID 57431513—
溶媒DimethylformamideHCID 6228—
生成物N-[6-(Dimethylamino)pyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamideHCID 24855800—

反応手順

0.27 ml (1.67 mmol) of diethyl cyanophosphonate is added dropwise at 20° C. under argon to a solution of 0.4 g (1.39 mmol) of 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acid (obtained in Example 1.1) and 0.229 g (1.67 mmol) of 3-amino-6-(dimethylamino)pyridine in 3.5 ml of dry dimethylformamide. The mixture is stirred for 10 minutes and then 0.43 ml (3.06 mmol) of triethylamine is added dropwise. The mixture is stirred at ambient temperature for 18 hours and concentrated under reduced pressure, and then the residue is taken up in 50 ml of ethyl acetate. This solution is then successively washed with three times 20 ml of a saturated sodium hydrogencarbonate solution, 50 ml of water and 20 ml of a saturated sodium chloride solution and then dried over sodium sulfate, filtered and concentrated under reduced pressure. The solid obtained is triturated from hot isopropyl ether. 0.423 g of a solid is collected by filtration, which solid is dried under reduced pressure and used as in the following stage.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481745B2
出典データセットuspto-grants-2013_07
ORD IDord-67b8ef6dddf342d9aa08ef3e16317729
出典メモuspto-grants-2013_07