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HRID 533394作成日:2026年10月25日

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

https://huagongshe.com/reaction/533394

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium hydrideHCID 24758—
反応物Benzene, 1,2-dichloro-3-fluoro-HCID 119011—
反応物3-(1-Hydroxy-3-methylsulfanylpropyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 66859760—
溶媒Hydrochloric AcidHCID 313—
溶媒DimethylformamideHCID 6228—
生成物3-[1-(2,3-Dichlorophenoxy)-3-methylsulfanylpropyl]pyrrolidineHCID 58120263—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853255B2
出典データセットuspto-grants-2014_10
ORD IDord-ff3710af2af542d9b93adc09216c8dd3
出典メモuspto-grants-2014_10