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HRID 10338作成日:2026年10月26日

Hydrochloric Acid → (7,8-Difluoro-3-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)-oxoacetaldehyde oxime

https://huagongshe.com/reaction/10338

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Chloral HydrateHCID 2707—
反応物Sodium sulfate decahydrateHCID 62649—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物7,8-Difluoro-2,3-dihydro-3-methyl-4H-(1,4)benzoxazineHCID 10219718—
溶媒WaterHCID 962—
生成物(7,8-Difluoro-3-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)-oxoacetaldehyde oximeHCID 73857481—

反応条件

温度77.5 °C

反応手順

A solution of 8.27 g (50 mmol) of chloral hydrate in 125 mL of water is treated with 112.8 g (0.35 mmol) of sodium sulfate decahydrate. The mixture is stirred and treated with a solution of 7,8-difluoro-3-methyl-3,4-dihydro-2H-benz[1,4]oxazine (Chem. Pharm. Bull., 1984; 32:4907) hydrochloride (prepared by dissolving 8.26 g (44.6 mmol) of the free base in 50 mmol of concentrated hydrochloric acid in 70 mL of 50% aqueous ethanol). The reaction is stirred and a solution of 9.8 g (140 mmol) of hydroxylamine hydrochloride in 50 mL of water is added. After heating at 75 to 80° C. for 3 hours, the reaction is stirred at room temperature overnight. The resulting precipitate is removed by filtration, washed with water, and the wet filter cake is dissolved in dichloromethane. The organic solution is washed with water, dried (MgSO4), decolorized with charcoal, filtered and concentrated in vacuo to give 10.5 g of the title compound, mp 188–190° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094780B1
出典データセットuspto-grants-2006_08
ORD IDord-b845dd2edd604c6ea501e182a83263a2
出典メモuspto-grants-2006_08