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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13449생성일: 2026년 10월 24일

Tert-butyl 4-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-2-carboxylate → 4-{2-[(4-Bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-2-carboxylic acid

https://huagongshe.com/ko/reaction/13449

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl 4-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-2-carboxylateHCID 22041284—
촉매WaterHCID 962—
용매Trifluoroacetic acidHCID 6422—
생성물4-{2-[(4-Bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-2-carboxylic acidHCID 22040646—

반응 단계

A solution of the product of step 7 in trifluoroacetic acid was treated with two drops of water at room temperature for 3-4 hours or until the reaction was determined to be complete by HPLC. The reaction was evaporated under reduced pressure to afford the product as a red-orange oil in quantitative yield. MS: MH+=439.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728010B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-33af28af016b497fa6bf2bf439a5eae2
출처 메모uspto-grants-2010_06