돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42190생성일: 2026년 10월 25일

Triethylamine → (S)-4-(5-Methoxycarbonyl-4-trifluoromethyl-pyrimidin-2-yl)-piperazine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl-ester

https://huagongshe.com/reaction/42190

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-tert-butyl 3-methyl (3S)-piperazine-1,3-dicarboxylateHCID 1501855—
반응물Methyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylateHCID 3696469—
용매1,4-DioxaneHCID 31275—
생성물(S)-4-(5-Methoxycarbonyl-4-trifluoromethyl-pyrimidin-2-yl)-piperazine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl-esterHCID 6870729061%

반응 단계

Combine 2-Chloro-4-trifluoromethyl-pyrimidine-5-carboxylic acid methyl ester (240 mg, 1.70 mmol), (S)-piperazine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester (2.04 mmol) and triethylamine (5.11 mmol) in a 0.85 M solution of dioxane. Microwave reaction mixture for 30 min at 150° C. Filter reaction mixture and rinse with acetonitrile. Purify filtrate by column chromatography in a 0-70% ethyl acetate/heptane gradient to give (S)-4-(5-Methoxycarbonyl-4-trifluoromethyl-pyrimidin-2-yl)-piperazine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl-ester contaminated with approximately 15% of the mono hydrolysis product. The mixture is carried on to next step without further purification. (61% yield)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536168B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-eb9edd583b6146c588dccfa774168ab9
출처 메모uspto-grants-2013_09