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HRID 406533作成日:2026年10月25日

Cesium carbonate → Methyl 2-[(tert-butoxycarbonyl)amino]-4-(3-chlorophenyl)-5-oxohexanoate

https://huagongshe.com/reaction/406533

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物1-(3-Chlorophenyl)propan-2-oneHCID 2734097—
反応物(S)-Methyl 2-Boc-amino-3-iodopropionateHCID 11416215—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-[(tert-butoxycarbonyl)amino]-4-(3-chlorophenyl)-5-oxohexanoateHCID 68750611—

反応手順

A mixture of cesium carbonate (9.80 g, 30.1 mmol) and methyl N-(tert-butoxycarbonyl)-3-iodo-D-alaninate (9.90 g, 30.1 mmol) in DMF (75 mL) was stirred at 23° C. for 45 min before 1-(3-chlorophenyl)propan-2-one (6.09 g, 36.1 mmol) and additional cesium carbonate (9.80 g, 30.1 mmol) were added. The resulting mixture was stirred for 2.5 h. The majority of the DMF was then removed under reduced pressure at a bath temperature of <40° C. The concentrated mixture was partitioned between water (500 mL) and ethyl acetate (2×200 mL). The combined organic layers were washed with brine, dried over sodium sulfate and concentrated to give the title compound as a 1:1 racemic mixture of diastereomers, which was used without further purification. MS: m/z=314.1 (M−t-Bu+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754096B2
出典データセットuspto-grants-2014_06
ORD IDord-37c15dd8ebb14f0aa59282d46c205bb0
出典メモuspto-grants-2014_06