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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1844963생성일: 2026년 10월 26일

Benzyl Bromide → 2-amino-1-benzyl-1H-benzoimidazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1844963

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물methyl 2-amino-1H-benzo[d]imidazole-4-carboxylateHCID 24730367—
용매Dimethyl SulfoxideHCID 679—
생성물2-amino-1-benzyl-1H-benzoimidazole-4-carboxylic acid methyl esterHCID 6694032055%

반응 단계

To a solution of 0.1 g (0.52 mmol) of 2-amino-1H-benzoimidazole-4-carboxylic acid methyl ester (intermediate A) in DMSO (1 mL) was added 0.089 g (0.52 mmol) of benzyl bromide, the reaction mixture was stirred at room temperature for 3 h. The conversion was monitored by LCMS. After usual work up, the residue was purified by column chromatography eluting with DCM/methanol (v/v=10:1) to afford 0.08 g (55%) of 2-amino-1-benzyl-1H-benzoimidazole-4-carboxylic acid methyl ester. LCMS: 281 (M+1)+; 1H NMR (DMSO-d6, 400 MHz): δ 7.49 (dd, 1H), 7.29 (t, 2H), 7.25 (m, 2H), 7.16(m, 2H), 7.05 (bs, 2H), 6.85 (t, 1H), 5.28 (s, 2H), 3.79 (s, 3H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08946259B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-35d29f11ad5d4d4daf296e8fd7e8748b
출처 메모uspto-grants-2015_02