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HRID 448826作成日:2026年10月26日

N2,N2-dimethylpyridine-2,5-diamine → N-[6-(Dimethylamino)pyridin-3-yl]-5-trifluoromethyl-1-(3-fluorobenzyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/448826

反応式

関与物質

役割名称HCID仕込み量
反応物N2,N2-dimethylpyridine-2,5-diamineHCID 78642—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物5-trifluoromethyl-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acidHCID 57431532—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-[6-(Dimethylamino)pyridin-3-yl]-5-trifluoromethyl-1-(3-fluorobenzyl)-1H-indole-2-carboxamideHCID 6893275340%

反応手順

0.185 g (1.35 mmol) of 3-amino-6-(dimethylamino)pyridine (WO2005/028452) in 2 ml of dry dimethylformamide is added dropwise at 20° C. under argon to a solution of 0.35 g (1.04 mmol) of 5-trifluoromethyl-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acid (WO2006/072736), 0.198 g (1.14 mmol) of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride and 0.165 g (1.14 mmol) of 1-hydroxybenzotriazole monohydrate in 6 ml of dry dimethylformamide. The reaction mixture is stirred overnight, run onto 100 ml of water and then extracted three times with 50 ml of ethyl acetate. The organic phases are subsequently combined, washed three times with 20 ml of water, dried over sodium sulfate and then concentrated under reduced pressure. The expected product is purified by chromatography on a silica column, elution being carried out with a mixture of dichloromethane and methanol. 0.19 g of the expected compound is thus isolated.

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-89c7f669a6874a82bdac977b98c3e5e8
出典メモuspto-grants-2013_07