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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37125생성일: 2026년 10월 26일

Sodium hydride → 2-(3,4-dihydro-2,2-dimethyl-7-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide

https://huagongshe.com/reaction/37125

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Bromopyridine 1-oxide hydrochlorideHCID 2724044—
반응물2,2-Dimethyl-7-nitro-3,4-dihydro-2H-benzo[B][1,4]oxazineHCID 10488570—
용매DimethylformamideHCID 6228—
생성물2-(3,4-dihydro-2,2-dimethyl-7-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxideHCID 1056619123.5%

반응 조건

온도70 °C

반응 단계

In 14 ml of N,N-dimethylformamide was suspended 0.38 g of sodium hydride (60% in oil) followed by addition of 1.00 g of 3,4-dihydro-2,2-dimethyl-7-nitro-2H-1,4-benzoxazine. Then, 1.01 g of 2-bromopyridine N-oxide hydrochloride was added with ice-cooling and the mixture was stirred at 70° C. for 16 hours. The reaction mixture was poured in ice-water and extracted with ethyl acetate. The organic layer was washed with aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was subjected to silica gel column chromatography and elution was carried out with chloroform-acetone (3:1) to give 0.34 g of 2-(3,4-dihydro-2,2-dimethyl-7-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide as oil. Then, a solution of hydrochloric acid in ethanol (prepared from 1 ml of concentrated hydrochloric acid and 5 ml of ethanol) was added thereto and the solvent was distilled off. The resulting residue wad recrystallized from acetone to give 182 mg of 2-(3,4-dihydro-2,2-dimethyl-7-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420126
출처 데이터셋uspto-grants-1995_05
ORD IDord-2cdbbf7a2ff64de481fa31b88634e9f2
출처 메모uspto-grants-1995_05