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HRID 1016081作成日:2026年10月27日

4-Hydroxy-4-phenylcyclohexan-1-one → N-(2-{[3-(Fluoromethyl)-1-(4-hydroxy-4-phenylcyclohexyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1016081

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydroxy-4-phenylcyclohexan-1-oneHCID 583741—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物N-(2-{[3-(fluoromethyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamideHCID 59556164—
溶媒DichloromethaneHCID 6344—
生成物N-(2-{[3-(Fluoromethyl)-1-(4-hydroxy-4-phenylcyclohexyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamideHCID 5955616716.7%

反応手順

100 mg (0.53 mmol) of 4-hydroxy-4-phenylcyclohexanone and 184 mg (0.53 mmol) of N-(2-{[3-(fluoromethyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide were dissolved in 10 mL of methylene chloride. To the solution was added 221 mg (1.06 mmol) of sodium triacetoxyborohydride. The reaction mixture was stirred at room temperature for 2 h. Direct chromatography on silica gel gave the final desired product 41 mg (top spot on TLC and first peak on HPLC, yield: 16.7%, MS: 522 (M+1)+) and the other isomer 51 mg (second peak on HPLC, yield: 20%, MS: 522 (M+1)+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07985730B2
出典データセットuspto-grants-2011_07
ORD IDord-fc1a93ac62284f06a8a884c8a37069d5
出典メモuspto-grants-2011_07