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HRID 533387作成日:2026年10月24日

Ethanol → (R)-3-[(S)-(2,3-Dichlorophenoxy)(tetrahydropyran-4-yl)-methyl]pyrrolidine

https://huagongshe.com/ja/reaction/533387

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(R)-3-[(S)-Hydroxy(tetrahydropyran-4-yl)methyl]pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 66859077—
溶媒Hydrochloric AcidHCID 313—
溶媒DimethylformamideHCID 6228—
生成物(R)-3-[(S)-(2,3-Dichlorophenoxy)(tetrahydropyran-4-yl)-methyl]pyrrolidineHCID 58120262—

反応手順

(R)-3-[(S)—Hydroxy(tetrahydropyran-4-yl)methyl]pyrrolidine-1-carboxylic acid t-butyl ester (30 mg, 0.1 mmol) was dissolved in DMF (380 μL). NaH (3.0 mg, 126 μmol) was added and the mixture was stirred at room temperature for 15 minutes. 1,2-Dichloro-3-fluorobenzene (34.7 mg, 210 μmol) was added and the mixture was stirred at 100° C. overnight. The mixture was concentrated then dissolved in 1.2M HCl in EtOH (510 μL, 610 μmol) and stirred overnight. The product was concentrated and purified by preparative HPLC to yield the title compound as a mono-TFA salt (10.8 mg, purity 100%). MS m/z: [M+H]+ calcd for C16H21Cl2NO2, 330.10. found 330.0.

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-d356a532631b4ee98e6bfc7899d2e29d
出典メモuspto-grants-2014_10