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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13515생성일: 2026년 10월 25일

4-Fluorophenyl isothiocyanate → 4-[2-(4-Fluoro-phenylamino)-1-methyl-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/13515

반응식

참여 물질

역할이름HCID투입량
반응물4-Fluorophenyl isothiocyanateHCID 15241—
반응물Tert-butyl4-[3-amino-4-(methylamino)phenoxy]pyridine-2-carboxylateHCID 22040526—
용매MethanolHCID 887—
생성물4-[2-(4-Fluoro-phenylamino)-1-methyl-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid tert-butyl esterHCID 21037368—

반응 단계

A round bottom flask was charged with 4-fluorophenylisothiocyanate (1 eq), 4-(3-Amino-4-methylamino-phenoxy)-pyridine-2-carboxylic acid tert-butyl ester (1 eq), and MeOH. The reaction was maintained stirring at room temperature overnight. Ferric chloride, (1.5 eq) was added and the resulting mixture was stirred overnight. The reaction was partitioned with EtOAc and water, and filtered through Celite. The layers were separated and the aqueous phase was neutralized with saturated Na2CO3 solution. The resulting aqueous phase was extracted with EtOAc and the mixture was filtered through Celite. The phases were separated and the aqueous phase was again extracted and filtered. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated to give a brown solid. The crude residue was purified by trituration in hot toluene to furnish the desired product. LCMS m/z 435.6 (MH+), tR=2.12 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728010B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-80899cb114014d05a92452156dc1b435
출처 메모uspto-grants-2010_06