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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1454985생성일: 2026년 10월 25일

1-Cinnamylpiperazine → 2-(Ethoxy)-2-oxoethyl trans-4-(3-phenylprop-2-en-1-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1454985

반응식

참여 물질

역할이름HCID투입량
반응물1-CinnamylpiperazineHCID 726896—
반응물Ethyl [(phenoxycarbonyl)oxy]acetateHCID 12094709—
용매TolueneHCID 1140—
생성물2-(Ethoxy)-2-oxoethyl trans-4-(3-phenylprop-2-en-1-yl)piperazine-1-carboxylateHCID 6730551635.3%

반응 단계

A solution of 1.40 g (6.93 mmol) of trans-1-cinnamylpiperazine and 1.74 g (7.76 mmol) of ethyl{[(phenoxy)carbonyl]oxy}acetate (J. Med. Chem., 1999, 42, 277-290) in 15 ml of toluene is heated at 80° C. overnight. It is evaporated to dryness and the residue is taken up in 50 ml of ethyl acetate. It is washed with 2 times 20 ml of water and 1 times 10 ml of saturated aqueous sodium chloride solution. It is dried over sodium sulphate and evaporated to dryness. The residue is purified by chromatography on silica gel, eluting with a 50/50 mixture of cyclohexane and ethyl acetate, then with ethyl acetate, to give 0.814 g of product in the form of a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07482346B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-33fefda3eeda40a3914791a5e94b15c1
출처 메모uspto-grants-2009_01