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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1197763생성일: 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/1197763

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

To a suspension of 0.38 g sodium hydride (60% in paraffin composition) in 14 ml dimethylformamide, was added 1.00 g 3,4-dihydro-2,2-dimethyl-7-nitro-2H-1,4-benzoxazine, and 1.01 g 2-bromopyridine N-oxide hydrochloride was further added under ice-cooling, and the mixture was stirred for 16 hours at 70° C. The reaction mixture was poured to ice water, the resulting mixture was extracted with ethyl acetate, and the extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was distilled off from the dried solution under reduced pressure, the residue was subjected to column chromatography on silica gel, and elution was conducted by the use of a 3:1 mixture of chloroform and acetone, thus giving 0.34 g of 2-(3,4-dihydro-2,2-dimethyl-7-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide. Ethanolic solution of hydrogen chloride (a mixture of 1 ml concentrated hydrochloric acid and 5 ml ethanol) was then added to the product obtained above, the solvent was distilled off from the mixture, and the residue was recrystallized from acetone, thus giving 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 번호US05278158
출처 데이터셋uspto-grants-1994_01
ORD IDord-d2e82f3fbc884c37aecafc5235c8fad4
출처 메모uspto-grants-1994_01