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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48024생성일: 2026년 10월 23일

Potassium Carbonate → [4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]phenyl]methyl-propanedioic acid, dimethyl ester

https://huagongshe.com/ko/reaction/48024

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물alpha,alpha-Diphenyl-4-pyridinemethanolHCID 74177—
반응물[4-(4-Chloro-1-oxobutyl)phenyl]methyl-propanedioic acid, dimethyl esterHCID 86585530—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물[4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]phenyl]methyl-propanedioic acid, dimethyl esterHCID 8658553176%

반응 단계

Mix together [4-(4-chloro-1-oxobutyl)phenyl]methyl-propanedioic acid, dimethyl ester (300 mg, 0.92 mmol), potassium carbonate (350 mg, 2.5 mmol), α-(4-pyridyl)benzhydrol (500 mg, 1.9 mmol), water (3 mL) and toluene (7 mL). Heat the mixture to reflux. After 5 days, cool to room temperature. Add ethyl acetate and water. Wash the organic phase with brine, dry over anhydrous magnesium sulfate and concentrate. Purify by flash chromatography (150 g of silica gel, 10% methanol/chloroform as eluent) to give the title compound (387 mg, 76%). Additionally, compounds derived from all permutations of substituents as set forth in the illustrative examples following Step F can be prepared by the synthetic procedure depicted in Step H.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06700012B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-e67c60553e744b948d31f3eda76ee3ea
출처 메모uspto-grants-2004_03