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HRID 1162530作成日:2026年10月25日

Water → 5-(2-Chloro-4-methoxycarbonylmethyl-phenyl)-3-phenyl-isoxazole-4-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1162530

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物AcetonitrileHCID 6342—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物3-(2-Chloro-4-methoxycarbonylmethyl-phenyl)-3-oxo-propionic acid tert-butyl esterHCID 68648183—
生成物5-(2-Chloro-4-methoxycarbonylmethyl-phenyl)-3-phenyl-isoxazole-4-carboxylic acid tert-butyl esterHCID 68648358—

反応手順

Intermediate 56 (115 mg, 0.35 mmol) is dissolved in MeCN (3 mL). Potassium bis(trimethylsilyl)amide (106 mg, 0.53 mmol) is added slowly while stirring at room temperature. Then the mixture is cooled to 0° C., and a solution of intermediate 58 (55 mg, 0.35 mmol) in CH3CN (1 mL) is added. The mixture is stirred at room temperature overnight, then H2O (5 mL) is added and the mixture is extracted with DCM (3×10 mL). After concentration the crude product is purified on reverse phase HPLC (H2O/MeCN gradient) to afford 5-(2-chloro-4-methoxycarbonylmethyl-phenyl)-3-phenyl-isoxazole-4-carboxylic acid tert-butyl ester 59 as a white solid: 1H-NMR (400 MHz, CDCl3) δ=7.73 (m, 2H), 7.47 (m, 5H), 7.33 (m, 1H), 3.72 (s, 3H), 3.68 (s, 2H), 1.23 (s, 9H). MS calculated for C23H23ClNO5 (M+H+) 428.1, found 428.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07820705B2
出典データセットuspto-grants-2010_10
ORD IDord-9dba909da1734a5288f9b1aeb9070b87
出典メモuspto-grants-2010_10