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HRID 1820176作成日:2026年10月26日

4-(4-Chlorophenyl)-4-hydroxypiperidine → N-(1-(4-(4-Chlorophenyl)-4-hydroxypiperidin-1-yl)-4-(methylthio)-1-oxobutan-2-yl)benzamide

https://huagongshe.com/reaction/1820176

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
反応物3-Methyl-2-(phenylformamido)butanoic acidHCID 226682—
反応物Benzoyl-dl-methionineHCID 295480—
反応物4-(4-chlorophenyl)piperidine HydrochlorideHCID 2757843—
生成物N-(1-(4-(4-Chlorophenyl)-4-hydroxypiperidin-1-yl)-4-(methylthio)-1-oxobutan-2-yl)benzamideHCID 57889006—

反応手順

Example 217 was prepared in a similar manner as described for the preparation of Example 208 with the exceptions that benzoyl-DL-methionine and 4-(4-chlorophenyl)-4-hydroxypiperidine were substituted for benzoyl-DL-valine and 4-(4-chlorophenyl)piperidine hydrochloride, respectively. MS found: (M+H)+=448.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07601844B2
出典データセットuspto-grants-2009_10
ORD IDord-54dde8d92b244532a474e24aaaae48ed
出典メモuspto-grants-2009_10