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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1460086생성일: 2026년 10월 26일

(2S,5S)-2,5-dimethylpiperazine → N,N-diethyl-4-(3-(tert-butyldimethylsilyloxy)-alpha-((2S,5S)-2,5-dimethyl-1-piperazinyl)benzyl)benzamide

https://huagongshe.com/reaction/1460086

반응식

참여 물질

역할이름HCID투입량
반응물(2S,5S)-2,5-dimethylpiperazineHCID 61380—
반응물4-(3-(tert-butyldimethylsilyloxy)-alpha-chlorobenzyl)-N,N-diethylbenzamideHCID 22350036—
반응물L-Ala-L-Ala diketopiperazineHCID 131720131—
용매TolueneHCID 1140—
생성물N,N-diethyl-4-(3-(tert-butyldimethylsilyloxy)-alpha-((2S,5S)-2,5-dimethyl-1-piperazinyl)benzyl)benzamideHCID 2294084022.1%

반응 단계

A mixture of 15.65 g (36 mmol) of N,N-diethyl-4-(3-(t-butyldimethylsilyloxy)-α-chlorobenzyl)benzamide, prepared as described in Example 11, 7.22 g (65 mmol) of (+)-(2S,5S)-2,5-dimethylpiperazine, prepared from L-Ala-L-Ala-diketopiperazine (Bachem Chemicals, Philadelphia, Pa.) as described by Jung and Rohloff (J. Org. Chem. 50, 4909-13 (1985)), and 3 mL of toluene was heated as in Example 1. The product was purified by chromatography on silica gel (Waters Prep 500 with dichloromethane containing 1% ethanol and 0.1% triethylamine) to give 4.06 g (22%) of N,N-diethyl-4-(3-(tert-butyldimethylsilyloxy)-α-((2S,5S)-2.5-dimethyl-1-piperazinyl)benzyl)benzamide as a beige foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05854249
출처 데이터셋uspto-grants-1998_12
ORD IDord-164e355ecd3b43879fde3bb9d55bff59
출처 메모uspto-grants-1998_12