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HRID 374800作成日:2026年10月25日

Dichloromethane → N-(2-[4-(Phenylmethyl)-1-piperazinyl]ethyl)tricyclo[3,3,1,13,7]-decane-1-carboxamide Dihydrochloride

https://huagongshe.com/reaction/374800

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物TriethylamineHCID 8471—
反応物1-Adamantanecarboxylic acidHCID 13235—
反応物Diethyl cyanophosphonateHCID 76257—
反応物2-(4-Benzylpiperazin-1-yl)ethan-1-amineHCID 2735331—
生成物N-(2-[4-(Phenylmethyl)-1-piperazinyl]ethyl)tricyclo[3,3,1,13,7]-decane-1-carboxamide DihydrochlorideHCID 4526246210%

反応手順

To a solution of adamantane-1-carboxylic acid (11.85 g, 0.065 mol) and 2-[4-(phenylmethyl)-1-piperazinyl]ethylamine (12.0 g, 0.054 mol) in dichloromethane (200 mL) at 4° C. was added, with stirring, a solution of diethylcyanophosphonate (11.8 mL, 0.065 mol) in dichloromethane (50 mL), followed by a solution of triethylamine (9.2 mL, 0.065 mol) in dichloromethane (50 mL). The resulting mixture was stirred overnight, during which time it came up to room temperature. The reaction mixture was then washed with 10% aqueous potassium carbonate (200 mL), dried over anhydrous sodium sulfate, and concentrated on a rotary evaporator. The desired product (TLC on silica gel using 10% methanol/ethyl acetate, Rf=0.33) was isolated by crystallization from hexane and recrystallized from hexane. It was then converted to its dihydrochloride salt with isopropanolic HCl (12.71 g, 52%), mp=259°-260° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05482940
出典データセットuspto-grants-1996_01
ORD IDord-21a31f10c9174edc9ce0b400497f97a7
出典メモuspto-grants-1996_01