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HRID 2421881作成日:2026年10月25日

HCID 57896640、化合物 → methyl 2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylate

https://huagongshe.com/reaction/2421881

反応式

関与物質

役割名称HCID仕込み量
反応物HCID 57896640HCID 57896640—
溶媒TetrahydrofuranHCID 8028—
生成物methyl 2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylateHCID 5789676586.4%

反応手順

To a suspension of methyl 2-oxo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylate (1.24 g, 5.96 mmol) in THF (30 mL) at 0° C. was added borane-tetrahydro-furan complex (23.83 mL, 23.83 mmol). The reaction was warmed to room temperature and allowed to stir for 2 hours. LCMS analysis of the reaction mixture indicated consumption of starting material. The reaction was chilled to 0° C. and quenched slowly with MeOH (20 mL). The reaction mixture was concentrated in vacuo and the treated with 5% sulfuric acid in MeOH (50 mL). The solution was heated to reflux for 1 hour. The solvent was removed under reduced pressure and the resulting oil was dissolved in EtOAc (100 mL) and washed successively with saturated aqueous NaHCO3 (2×50 mL) and brine (50 mL). The combined organics were dried over anhydrous Na2SO4 and concentrated in vacuo to provide methyl 2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylate (1 g, 5.15 mmol, 86% yield) as a white solid. The product was used without purification. LCMS (+ESI) m/z=195.0 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07960377B2
出典データセットuspto-grants-2011_06
ORD IDord-931a6ef5827e4b5385b432fb503cfa80
出典メモuspto-grants-2011_06