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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448826생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물N2,N2-dimethylpyridine-2,5-diamineHCID 78642—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물5-trifluoromethyl-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acidHCID 57431532—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-[6-(Dimethylamino)pyridin-3-yl]-5-trifluoromethyl-1-(3-fluorobenzyl)-1H-indole-2-carboxamideHCID 6893275340%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481745B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-89c7f669a6874a82bdac977b98c3e5e8
출처 메모uspto-grants-2013_07