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HRID 1472497作成日:2026年10月26日

Acetic Anhydride → rac-Linezolid

https://huagongshe.com/reaction/1472497

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物Tetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
反応物3-Fluoro-4-morpholinylphenyl-5-aminomethyl-1,3-oxazolidin-2-oneHCID 22714579—
溶媒DichloromethaneHCID 6344—
生成物rac-LinezolidHCID 392985%

反応手順

To a reaction flask were added 6.53 mmol of dihydrochloride of 3-(3-fluoro-4-morpholinylphenyl-5-aminomethyl-1,3-oxazolidin-2-one (5a), 100 ml of dichloromethane and 2.95 ml (21.2 mmol) of triethylamine. Then 0.8 ml (8.45 mmol) of acetic anhydride was added while being stirred in an ice-bath. The mixture was then allowed to react at room temperature for 2 hours before being washed successively with 5% aqueous NaOH solution and saturated aqueous NaCl solution. The organic layer was then dried by anhydrous sodium sulfate and filtered, and subsequently put under reduced pressure for solvent removal. The residue was then subjected to recrystallization using ethyl acetate to give white needle crystals at a yield of 85%, HR-TOF-MS (+Q) m/z: 338.1520 (Calculated [C16H20FN3O4+H]+: 338.1516).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09012631B2
出典データセットuspto-grants-2015_04
ORD IDord-105550dc7a56445f8ca6182f96d8c40a
出典メモuspto-grants-2015_04