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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533394생성일: 2026년 10월 24일

Ethanol → 3-[1-(2,3-Dichlorophenoxy)-3-methylsulfanylpropyl]pyrrolidine

https://huagongshe.com/ko/reaction/533394

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium hydrideHCID 24758—
반응물Benzene, 1,2-dichloro-3-fluoro-HCID 119011—
반응물3-(1-Hydroxy-3-methylsulfanylpropyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 66859760—
용매Hydrochloric AcidHCID 313—
용매DimethylformamideHCID 6228—
생성물3-[1-(2,3-Dichlorophenoxy)-3-methylsulfanylpropyl]pyrrolidineHCID 58120263—

반응 단계

3-(1-Hydroxy-3-methylsulfanylpropyl)pyrrolidine-1-carboxylic acid t-butyl ester (49 mg, 180 μmol) was dissolved in DMF (550 μL). 60% NaH in oil (60:40, NaH:mineral oil, 8.5 mg, 210 μmol) was slowly added, and the mixture was stirred for 15 minutes at room temperature. 1,2-Dichloro-3-fluorobenzene (62 μL, 530 μmol) was added, and the resulting mixture was heated at 90° C. for 24 hours. The reaction was quenched with MeOH, and DMF/MeOH was removed in vacuo. The product was dissolved in 1.25M HCl in EtOH (1.4 mL, 1.8 mmol) and stirred overnight at room temperature. The product was then purified by preparative HPLC to yield the title compound as a mixture of all 4 stereoisomers (R,R, R,S, S,S, and S,R) as mono-TFA salts (20 mg, 100% purity). MS m/z: [M+H] calcd for C14H19Cl2NOS, 320.06. found 320.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853255B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-ff3710af2af542d9b93adc09216c8dd3
출처 메모uspto-grants-2014_10