돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1432905생성일: 2026년 10월 27일

Triphenyl Phosphate → (3S, 5R)-1-(2,4-dimethoxy-benzyl)-3,5-dimethyl-4-trifluoroacetyl-piperazin-2-one

https://huagongshe.com/reaction/1432905

반응식

참여 물질

역할이름HCID투입량
반응물Triphenyl PhosphateHCID 8289—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(2S, 2S)-N-(2,4-Dimethoxy-benzyl)-N-(2-hydroxypropyl)-2-(2,2,2-trifluoroacetylamino)-propionamideHCID 86592544—
용매TetrahydrofuranHCID 8028—
생성물(3S, 5R)-1-(2,4-dimethoxy-benzyl)-3,5-dimethyl-4-trifluoroacetyl-piperazin-2-oneHCID 5717147143.1%

반응 단계

(2S, 2S)-N-(2,4-Dimethoxy-benzyl)-N-(2-hydroxypropyl)-2-(2,2,2-trifluoroacetylamino)-propionamide (3.64 g, 9.29 mmol) is dissolved in 25 mL of tetrahydrofuran. Triphenylphosphate (3.65 g, 14.0 mmol) is added, and the resulting mixture is cooled to 0° C. before diethyl azodicarboxylate (2.2 mL, 14 mmol) is added slowly. The resulting mixture is left to stir overnight. The reaction mixture is condensed, and the residue is purified by column chromatography (SiO2, 25% ethyl acetate/hexane). The desired product, (3S, 5R)-1-(2,4-dimethoxy-benzyl)-3,5-dimethyl-4-trifluoroacetyl-piperazin-2-one (1.5 g, 43% yield), is isolated as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612075B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-d0c248c53bfe4d62a63af17d0d0d2e4c
출처 메모uspto-grants-2009_11