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HRID 37106作成日:2026年10月26日

Sodium hydride → 2-(3,4-Dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide

https://huagongshe.com/reaction/37106

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2-Bromopyridine 1-oxide hydrochlorideHCID 2724044—
反応物2,2-Dimethyl-6-nitro-3,4-dihydro-2H-benzo[B][1,4]oxazineHCID 10727057—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(3,4-Dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxideHCID 131974—

反応手順

In 10 ml of N,N-dimethylformamide was dissolved 2.66 g of 3,4-dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazine followed by addition of 1.02 g of sodium hydride (60% in oil) and the mixture was stirred at room temperature for 30 minutes. Then, 2.77 g of 2-bromopyridine N-oxide hydrochloride was added with ice-cooling and, after the evolution of heat had subsided, the mixture was stirred at room temperature for 2 hours. The reaction mixture was then poured in water and extracted with ethyl acetate. The organic layer was separated and dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and the residue was chromatographed on a silica gel column using chloroform as the eluent to give crude 2-(3,4-dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420126
出典データセットuspto-grants-1995_05
ORD IDord-43bd8fdba5d64894acdd9bc217ce5490
出典メモuspto-grants-1995_05