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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 342121생성일: 2026년 10월 24일

Triethylamine → N-Methyl-N-methoxy-2-(1-triphenylmethyl-1H-imidazol-4-yl)acetamide

https://huagongshe.com/ko/reaction/342121

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물BromotriphenylmethaneHCID 11692—
반응물Imidazole-4-acetic acidHCID 96215—
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-Methyl-N-methoxy-2-(1-triphenylmethyl-1H-imidazol-4-yl)acetamideHCID 54243787—

반응 단계

To a solution of 4-imidazoleacetic acid (1.04 g, 6.40 mmol) and triphenylmethyl bromide (2.48 g, 7.68 mmol) in dimethylformamide (40 ml) was added triethylamine (4.46 ml, 32 mmol) and the suspension allowed to stir for 18 hours at room temperature. After this time, the mixture was treated with 3-hydroxy-1,2,3-benzotriazin-4(3)-one (HOOBT) (1.31 g, 8 mmol), N, O-dimethylhydroxyamine hydrochloride (1.56 g, 16 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) (1.53 g, 8 mmol) and stirred for 24 hours at room temperature. After this time, sat. aq. sodium bicarbonate (50 ml) and water (50 ml) were added and the mixture was extracted with ethyl acetate (2×100 ml). The combined extracts were washed with sat. aq. NaHCO3 (100 ml) and then brine (50 ml) and the solvent evaporated in vacuo. The residue was suspended in ether (20 ml) and the white solid filtered to give the title compound as a white solid. 1NMR(CD3OD, 300 MHz) δ 7.37(10H, m), 7.16(6H, m), 6.84(1H, s), 3.73(2H, s), 3.68(3H, s) and 3.18(3H, s)ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05856326
출처 데이터셋uspto-grants-1999_01
ORD IDord-b17ad3e9309c4c468864fcd3b06c7b39
출처 메모uspto-grants-1999_01