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HRID 30187作成日:2026年10月24日

Potassium Carbonate → (RS)-3-[2-(4-Fluorophenyl)-2-oxo-ethoxycarbonylmethyl]piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ja/reaction/30187

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-Bromo-1-(4-fluorophenyl)ethan-1-oneHCID 96749—
反応物1-Fmoc-4-Boc-Piperazine-2-acetic acidHCID 2756796—
溶媒DimethylformamideHCID 6228—
生成物(RS)-3-[2-(4-Fluorophenyl)-2-oxo-ethoxycarbonylmethyl]piperazine-1-carboxylic acid tert-butyl esterHCID 67158269—

反応手順

(RS)-2-Carboxymethylpiperazine-1,4-dicarboxylic acid 4-tert-butyl ester 1-(9H-fluoren-9-ylmethyl) ester from description 109 (2.0 g) was dissolved in DMF (25 ml) and stirred at room temperature under argon for 3 days in the presence of potassium carbonate (0.697 g) and 2-bromo-4′-fluoroacetophenone (0.930 g). The reaction solution was then partitioned between ethyl acetate and water the organic solution was washed with brine, dried (MgSO4) and evaporated. The crude product was chromatographed over silica gel, eluting with 25 to 100% ethyl acetate in hexane, followed by 10% ethanol in ethyl acetate. The title compound was obtained as a pale yellow solid (0.887 g), mass spectrum (API+) 381 [MH+], C19H25FN2O5 requires 380.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423052B2
出典データセットuspto-grants-2008_09
ORD IDord-6becd9c209224681b3840be6c555f791
出典メモuspto-grants-2008_09