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HRID 563199作成日:2026年10月25日

Potassium Carbonate → (2R,3S)-2-(3-chloro-4-cyano-2-ethylphenylamino)-3-hydroxybutanoic acid

https://huagongshe.com/reaction/563199

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-Hydroxy-1,2,3-propanetricarboxylic acid hydrate (1:1)HCID 22230—
反応物D-ThreonineHCID 69435—
反応物2-Chloro-3-ethyl-4-fluorobenzonitrileHCID 57908695—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物(2R,3S)-2-(3-chloro-4-cyano-2-ethylphenylamino)-3-hydroxybutanoic acidHCID 67006383467.3%

反応手順

4-Fluoro-2-chloro-3-ethyl benzonitrile (1.0 g, 5.45 mmol), D-threonine (779 mg, 6.54 mmol), potassium carbonate (1.51 g, 10.9 mmol) and DMSO (6 mL) were heated at 85° C. for 17.5 h. The reaction mixture was allowed to cool to room temperature whereupon water (20 mL) was added followed by citric acid monohydrate (2 g). After stirring for 10 min the mixture was partitioned between EtOAc (40 mL) and water. The organic phase was then washed with water (15 mL), brine (15 mL), dried (Na2SO4) and concentrated to furnish a pale yellow solid (7.2 g). This crude product was then passed through a silica-plug [hexanes-EtOAc (95:5) as eluent] to furnish a white solid (928 mg), which was used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067448B2
出典データセットuspto-grants-2011_11
ORD IDord-c445dec7a86d4f418e70efbb44377c47
出典メモuspto-grants-2011_11