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HRID 15235作成日:2026年10月27日

Methyl 4-iodobenzoate → 1-tert-Butoxycarbonyl-4-[2-(4-methoxycarbonyl-phenylsulfanyl)-phenyl]-piperidine-4-ol

https://huagongshe.com/reaction/15235

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-iodobenzoateHCID 69273—
反応物4-Hydroxy-4-(2-mercapto-phenyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 68682215—
反応物1-Bromo-2-(4-chlorophenylsulfanyl)-5-(trifluoromethyl)benzeneHCID 68683413—
生成物1-tert-Butoxycarbonyl-4-[2-(4-methoxycarbonyl-phenylsulfanyl)-phenyl]-piperidine-4-olHCID 68683807—

反応手順

1-tert-Butoxycarbonyl-4-[2-(4-methoxycarbonyl-phenylsulfanyl)-phenyl]-piperidine-4-ol (intermediate for 4a) was prepared from 4-hydroxy-4-(2-mercapto-phenyl)-piperidine-1-carboxylic acid tert-butyl ester, and 4-iodo-benzoic acid methyl ester by the palladium-catalysed coupling procedure described for 1-bromo-2-(4-chloro-phenylsulfanyl)-5-(trifluoromethyl)-benzene.

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-e755c54ecda14b6e9ec408363ce84315
出典メモuspto-grants-2010_06