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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362132생성일: 2026년 10월 26일

1,2-Dichloroethane → (E)-3-[6-[N-(methoxycarbonylmethyl)amino]pyridin-3-yl]-N-methyl-N-(2-methyl-1H-indol-3-ylmethyl)acrylamide

https://huagongshe.com/reaction/1362132

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amineHCID 10954023—
반응물(e)-3-[6-[n-(Methoxycarbonylmethyl)amino]pyridin-3-yl]acrylic acid hydrochloride saltHCID 66905135—
용매dichloromethane N,N-dimethylformamideHCID 22350042—
생성물(E)-3-[6-[N-(methoxycarbonylmethyl)amino]pyridin-3-yl]-N-methyl-N-(2-methyl-1H-indol-3-ylmethyl)acrylamideHCID 1036310973%

반응 단계

To a stirred solution of (E)-3-[6-[N-(methoxycarbonylmethyl)amino]pyridin-3-yl]acrylic acid hydrochloride salt (2.0 g, 7.3 mmole) in 1:1 DMF/CH2Cl2 (100 mL) was added 2-methyl-3-(methylaminomethyl)indole (1.3 g, 7.5 mmole), Et3N (2.1 mL, 15 mmole), and HOBt.H2O (1.0 g, 7.4 mmole), followed by EDC (1.4 g, 7.3 mmole). After stirring at room temperature for 18 h the reaction was concentrated to dryness. The residue was taken up in EtOAc, and the solution was washed with H2O then brine, dried (Na2SO4), and concentrated under vacuum. The remaining residue was purified by flash chromatography on silica gel (4% MeOH/CHCl3) to give the title compound (2.08 g, 73%) as an off-white solid: MS (ES) m/e 393.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879872B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-ff1439cdb0a7451eb64cedb7468e66dc
출처 메모uspto-grants-2011_02