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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 524145생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → 3-({4-[3-(3,4-Dimethoxyphenyl)-4,4-dimethyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl]piperidin-1-yl}carbonyl)phenyl acetate

https://huagongshe.com/reaction/524145

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물3-Acetoxybenzoic acidHCID 238669—
반응물5-(3,4-dimethoxyphenyl)-4,4-dimethyl-2-piperidin-4-yl-2,4-dihydro-3H-pyrazol-3-one hydrochlorideHCID 66616406—
용매DichloromethaneHCID 6344—
생성물3-({4-[3-(3,4-Dimethoxyphenyl)-4,4-dimethyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl]piperidin-1-yl}carbonyl)phenyl acetateHCID 46202721—

반응 단계

A mixture of 10 g 5-(3,4-dimethoxyphenyl)-4,4-dimethyl-2-(piperidin-4-yl)-2,4-dihydro-3H-pyrazol-3-one (compound B1), 8 g of 3-(acetyloxy)benzoic acid and 7 g of DCC in 150 ml of DCM is stirred for 2 h until the reaction is complete according to TLC analysis. The reaction mixture is quenched with water, the phases are separated and the organic phase is washed with water again. The organic phase is dried over MgSO4, and the solvent is removed under reduced pressure resulting in a crude product, which is purified by crystallization from methanol to yield the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340522B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-00e8849f8046435882f0a5e8979fbacf
출처 메모uspto-grants-2016_05