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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393576생성일: 2026년 10월 23일

N,N-Diethylaniline → 1H-Indole-2-carboxamide

https://huagongshe.com/ko/reaction/393576

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiethylanilineHCID 7061—
반응물Indole-2-carboxylic acidHCID 72899—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매TetrahydrofuranHCID 8028—
생성물1H-Indole-2-carboxamideHCID 594832327%

반응 조건

온도23 °C

반응 단계

Diethylaniline (0.33 μL, 2.1 μmol, 1.1 equiv) was added in one portion to a stirred solution of the amine (1.0 mg, 1.9 μmol, 1 equiv) in THF (0.15 mL) at 0° C. under an argon atmosphere and the solution was stirred for 5 min. Indole-2-carboxylic acid (0.40 mg, 2.5 μmol, 1.3 equiv), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.48 mg, 2.5 μmol, 1.3 equiv) and 1-hydroxybenzotriazole (0.31 mg, 2.3 μmol, 1.2 equiv) were then added separately, each in one portion, to the above solution at 0° C. The reaction mixture was warmed to 23° C. over 15 h 30 min, then was quenched with saturated aqueous ammonium chloride solution (3 mL). The mixture was diluted with ethyl acetate (10 mL) and the layers were separated. The aqueous layer was extracted with ethyl acetate (10 mL) and the combined organic layer was dried over sodium sulfate. Concentration in vacuo left a white solid, which was purified by flash column chromatography (60% ethyl acetate-hexanes) to give the indole-2-carboxylic acid amide derivative (1.1 mg, 87%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809099B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-f6e0d1663bfc40c08267e40cb1de1039
출처 메모uspto-grants-2004_10