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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15232생성일: 2026년 10월 24일

Methyl iodide → 1-tert-Butoxycarbonyl-4-[2-(2-fluoro-4-methoxy-phenylsulfanyl)-5-fluoro-phenyl]-piperidine-4-ol

https://huagongshe.com/ko/reaction/15232

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물3-Fluoro-4-nitrophenolHCID 520948—
반응물4-Amino-3-fluorophenolHCID 2735919—
반응물2-Fluoro-1-iodo-4-methoxybenzeneHCID 21187203—
반응물4-(5-Fluoro-2-mercapto-phenyl)-4-hydroxy-piperidine-1-carboxylic acid tert-butyl esterHCID 68682113—
생성물1-tert-Butoxycarbonyl-4-[2-(2-fluoro-4-methoxy-phenylsulfanyl)-5-fluoro-phenyl]-piperidine-4-olHCID 68685410—

반응 단계

Prepared from 4-hydroxy-4-(2-mercapto-5-fluoro-phenyl)-piperidine-1-carboxylic acid tert-butyl ester and 2-fluoro-1-iodo-4-methoxy-benzene (prepared from 3-fluoro-4-nitro-phenol by reduction to 4-amino-3-fluoro-phenol as reported by Hogdson and Nicholson J. Chem. Soc. 1941, 645-646 followed by diazotization according to the general procedure by Tunney and Stille J. Org. Chem. 1987, 52, 748-753 followed by alkylation with methyl iodide according to the general procedure by Uozumi et al. J. Org. Chem. 1993, 58, 1945-1945).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732463B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-eb6764547d314c8091b2eae6455fe324
출처 메모uspto-grants-2010_06