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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13504생성일: 2026년 10월 23일

Methyl iodide → Methyl5-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-3-carboxylate

https://huagongshe.com/ko/reaction/13504

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물4-Bromophenyl isothiocyanateHCID 16133—
반응물Methyl5-[3-amino-4-(methylamino)phenoxy]pyridine-3-carboxylateHCID 22040511—
용매MethanolHCID 887—
생성물Methyl5-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-3-carboxylateHCID 22040538—

반응 단계

A solution of the methyl5-[3-amino-4-(methylamino)phenoxy]pyridine-3-carboxylate (1 eq) in methanol (8 ml) was treated with 4-bromophenylisothiocyanate (1 eq) and stirred at 60° C.-65° C. for 2 hours. The reaction mixture was cooled down to room temperature and methyl iodide (1 eq) was added and stirred overnight at 60° C. The reaction was cooled down to room temperature, evaporated, taken up in ethyl acetate and washed with water and brine, dried, evaporated under reduced pressure. Column chromatography yielded methyl5-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-3-carboxylate. MS: MH+=452

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728010B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1b337a0935334edbab9388c479de6e9a
출처 메모uspto-grants-2010_06