戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 15232作成日:2026年10月26日

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

https://huagongshe.com/reaction/15232

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物3-Fluoro-4-nitrophenolHCID 520948—
反応物4-Amino-3-fluorophenolHCID 2735919—
反応物2-Fluoro-1-iodo-4-methoxybenzeneHCID 21187203—
反応物4-(5-Fluoro-2-mercapto-phenyl)-4-hydroxy-piperidine-1-carboxylic acid tert-butyl esterHCID 68682113—
生成物1-tert-Butoxycarbonyl-4-[2-(2-fluoro-4-methoxy-phenylsulfanyl)-5-fluoro-phenyl]-piperidine-4-olHCID 68685410—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732463B2
出典データセットuspto-grants-2010_06
ORD IDord-eb6764547d314c8091b2eae6455fe324
出典メモuspto-grants-2010_06