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HRID 1943687作成日:2026年10月27日

Water → (2,3-Dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-(3-methoxy-isoxazol-5-yl)-methanone

https://huagongshe.com/reaction/1943687

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物3-Methoxy-5-isoxazolecarbonyl chlorideHCID 12196359—
反応物2H,3H,4H-pyrido[4,3-b][1,4]oxazineHCID 21885950—
溶媒DichloromethaneHCID 6344—
生成物(2,3-Dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-(3-methoxy-isoxazol-5-yl)-methanoneHCID 44608544—

反応手順

In a 10 ml flask, 3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazine (100 mg, 0.73 mmol) and 3-methoxy-isoxazol-5-carbonyl chloride (131 mg, 0.80 mmol) were dissolved in dichloromethane. Triethylamine (0.51 ml, 3.65 mmol) was added thereto and then stirred at room temperature for 2 hours. After completion of the reaction by adding water dropwise, the reaction mixture was extracted with dichloromethane, and the combined organic layer was dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by column chromatography on amine silica eluting with a solvent of dichloromethane:methanol=30:1. The fractions containing the product were collected and evaporated to obtain the target compound 43, i.e., (2,3-dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-(3-methoxy-isoxazol-5-yl)-methanone, as pale-brown solid (149 mg, 78%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394792B2
出典データセットuspto-grants-2013_03
ORD IDord-bf094ab021954322a9bee2d356e54902
出典メモuspto-grants-2013_03