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HRID 336209作成日:2026年10月26日

Phosphorus oxychloride → 3-(5-tert-Butyl-isoxazol-3-ylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/336209

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxychlorideHCID 24813—
反応物3-Isoxazolamine, 5-(1,1-dimethylethyl)-HCID 171473—
反応物4-(tert-Butoxycarbonyl)morpholine-3-carboxylic acidHCID 2760133—
溶媒PyridineHCID 1049—
生成物3-(5-tert-Butyl-isoxazol-3-ylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl esterHCID 86660402—

反応手順

To a cold (0° C.) solution of morpholine-3,4-dicarboxylic acid 4-tert-butyl ester (100 mg; 0.432 mmol) and 3-amino-5-t-butylisoxazole (58.9 mg; 0.42 mmol) in anhydrous pyridine (1.2 mL) is added phosphorous oxychloride (0.039 mL; 0.432 mmol). The reaction mixture is left stirring at room temperature for 1 hour. After this time, the reaction mixture is quenched with saturated NH4Cl aqueous solution and extracted with ethyl acetate twice. The organics are combined and washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. Purification by flash chromatography on silica gel using methanol/methylene chloride provides the title compound, m/z 354 [M+H+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889670B2
出典データセットuspto-grants-2014_11
ORD IDord-6942aa99a61e48f8a2405baa04cd22c5
出典メモuspto-grants-2014_11