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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1511473생성일: 2026년 10월 27일

Citric Acid → (2S,4R)-1-(tert-butoxycarbonyl)-4-(6-methoxy-3-methylisoquinolin-1-yloxy)pyrrolidine-2-carboxylic acid

https://huagongshe.com/reaction/1511473

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물1-(1,1-Dimethylethyl) (2S)-4-hydroxy-1,2-pyrrolidinedicarboxylateHCID 11138980—
반응물Potassium tert-butoxideHCID 23665647—
반응물1-Chloro-6-methoxy-3-methylisoquinolineHCID 57893095—
용매Dimethyl SulfoxideHCID 679—
생성물(2S,4R)-1-(tert-butoxycarbonyl)-4-(6-methoxy-3-methylisoquinolin-1-yloxy)pyrrolidine-2-carboxylic acidHCID 57893088—

반응 단계

N-BOC-4-hydroxy-L-proline (A; 281 mg; 1.21 mmol) was dissolved in dimethylsulfoxide (3 mL) at room temperature then potassium t-butoxide (270 mg; 2.4 mmol) was added. The resulting solution was stirred at room temperature for 2 hours, then cooled to 0° C. A solution of 1-chloro-6-methoxy-3-methylisoquinoline in dimethylsulfoxide (3 mL) was then added dropwise to the cold solution, followed by t-BuOK, and the mixture was allowed to warn to room temperature. The solution was stirred for 16 hours. The reaction mixture was acidified to pH=4 with 5% aq. citric acid. The solution was extracted with ethyl acetate and the organic phase washed with water followed by brine. The organic phase was concentrated under reduced pressure to give (2S,4R)-1-(tert-butoxycarbonyl)-4-(6-methoxy-3-methylisoquinolin-1-yloxy)pyrrolidine-2-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08211897B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-c0d6882bdf8740b1b82840f7788649d4
출처 메모uspto-grants-2012_07