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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1030617생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1030617

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물TriethylamineHCID 8471—
반응물1-Adamantanecarboxylic acidHCID 13235—
반응물Diethyl cyanophosphonateHCID 76257—
반응물2-(4-Benzylpiperazin-1-yl)ethan-1-amineHCID 2735331—
생성물N-(2-[4-(Phenylmethyl)-1-piperazinyl]ethyl)tricyclo[3,3,1,13,7]-decane-1-carboxamide DihydrochlorideHCID 4526246210%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05106849
출처 데이터셋uspto-grants-1992_04
ORD IDord-8c980e1938f44627838b33fe721e7a9f
출처 메모uspto-grants-1992_04