돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350743생성일: 2026년 10월 27일

1-Phenylpiperazine → 3-[4-(4-Chlorophenyl)-2-(4-phenyl-l-piperazinyl)-5-oxazolyl]propionic acid

https://huagongshe.com/reaction/350743

반응식

참여 물질

역할이름HCID투입량
반응물1-PhenylpiperazineHCID 7096—
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물2-Chloro-4-(4-chlorophenyl)-5-oxazolepropionic acidHCID 11808258—
용매DimethylformamideHCID 6228—
생성물3-[4-(4-Chlorophenyl)-2-(4-phenyl-l-piperazinyl)-5-oxazolyl]propionic acidHCID 2108864553%

반응 조건

온도100 °C

반응 단계

A mixture of 3-[2-chloro-4-(4-chlorophenyl)-5-oxazolyl]propionic acid (1.0 g), 1-phenylpiperazine (2.27 g), potassium carbonate (2.42 g) and N,N-dimethylformamide (20 mL) was stirred at 100° C. for 3 hrs. The reaction mixture was poured into aqueous ammonium chloride solution and the mixture was extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography and 3-[4-(4-chlorophenyl)-2-(4-phenyl-l-piperazinyl)-5-oxazolyl]propionic acid (0.76 g, yield 53%) was obtained as a powder from a fraction eluted with ethyl acetate-chloroform-methanol (10:10:1, volume ratio). Recrystallization from ethyl acetate gave colorless prism crystals. melting point: 177–178° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07183276B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-c70f9d88ad9b4b9e981f5d7c8d433fa1
출처 메모uspto-grants-2007_02