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HRID 567681作成日:2026年10月26日

Hydrochloric Acid → 2-(2,6-Difluoro-phenyl)-8-hydroxy-benzo[d][1,3]oxazin-4-one

https://huagongshe.com/reaction/567681

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2,6-Difluorobenzoyl chlorideHCID 87438—
反応物6-Acetamido-(2,6-difluoro-phenyl)-benzo[d][1,3]oxazin-4-oneHCID 9948813—
反応物HCID 21262505HCID 21262505—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
溶媒Toluene triethylamineHCID 22504574—
生成物2-(2,6-Difluoro-phenyl)-8-hydroxy-benzo[d][1,3]oxazin-4-oneHCID 9838451—

反応手順

3-Triisopropylsilyloxyanthranilic acid (0.8 g), 2,6-difluorobenzoyl chloride (0.71 mL) and triethyl amine/toluene (1/1) (25 mL) were reacted as described under (10). Reaction time 2 days. Extraction between ethyl acetate (100 mL) and HCl (1N,100 mL), followed by separation of the organic layer, drylng over MgSO4, filtering and evaporation gave a crude product which was dissolved in warm THF (20 mL) and precipitated with hexane. The resulting mixture was further purified on a silicagel column using dichloromethane as eluent. The isolated fraction (80 mg) was hydrolysed with 1% HCl in ethanol by stirring for 2 days at RT, and further hydrolysis after addition of HCl (4N, 5 mL) and ethyl acetate (10 mL). The organic layer was separated, evaporated and dried resulting in 2-(2,6-difluoro-phenyl)-8-hydroxy-benzo[d][1,3]oxazin-4-one (32 mg), mp.190-198. LC-MS showed the purity 86% with the corresponding O-triisopropylsilylated product as the impurity.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06180625B2
出典データセットuspto-grants-2001_01
ORD IDord-a184ea4c4a6b4c92bf8258b1217fc931
出典メモuspto-grants-2001_01