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HRID 57376作成日:2026年10月25日

Pyridine → (R)-N-methoxy-N-methyl-2-((S)-2-oxooxazolidin-4-yl)propanamide

https://huagongshe.com/reaction/57376

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物N,O-DimethylhydroxylamineHCID 14232—
反応物1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
反応物(R)-2-((S)-2-oxooxazolidin-4-yl)propanoic acidHCID 90416617—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒Sodium BicarbonateHCID 516892—
生成物(R)-N-methoxy-N-methyl-2-((S)-2-oxooxazolidin-4-yl)propanamideHCID 90416286195.4%

反応手順

To a mixture of (R)-2-((S)-2-oxooxazolidin-4-yl)propanoic acid (1.1 g, 6.91 mmol) in DCM (20 mL) was added 1-chloro-N,N,2-trimethylprop-1-en-1-amine (1.385 g, 10.37 mmol) at 0° C. The ice bath was removed and the mixture was stirred for 30 min at ambient temperature. A mixture of N,O-dimethylhydroxylamine (1.011 g, 10.37 mmol) and pyridine (1.677 mL, 20.74 mmol) in DCM (20 mL) was added and stirring was continued for ˜1 hr. The mixture was diluted with water (˜2 mL) and saturated sodium bicarbonate solution (˜2 mL) and stirred for ˜15 min. The mixture was diluted with dichloromethane (˜30 mL). The separated aqueous layer was extracted with DCM (1×), the organic layers were combined, dried over sodium sulfate, filtered and concentrated under reduced pressure providing crude (R)—N-methoxy-N-methyl-2-((S)-2-oxooxazolidin-4-yl)propanamide (2.73 g) as an orange oil which was directly used without further purification. MS m/z 203.1 (M+H)+; Rt-0.36 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434719B2
出典データセットuspto-grants-2016_09
ORD IDord-8c0f8c9063684160acbc4c11b31cdc50
出典メモuspto-grants-2016_09