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HRID 588732作成日:2026年10月26日

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

https://huagongshe.com/reaction/588732

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 ambient temperature 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 in vacuo 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US09227972B2
出典データセットuspto-grants-2016_01
ORD IDord-2f0ad1b48fd14a2eac2dae56112ed563
出典メモuspto-grants-2016_01