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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2073196생성일: 2026년 10월 26일

Hydrogen Peroxide → 5-(2-Methylpropyl)-8-[3-(trifluoromethyl)phenyl]-3H,6H-1,4,5a,8a-tetraazaacenaphthylen-3-one

https://huagongshe.com/reaction/2073196

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참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물IsobutylamineHCID 6558—
반응물Sodium HydroxideHCID 14798—
반응물4,5-Dihydro-5-thioxo-8-(3-(trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3-oneHCID 15044079—
용매DimethylformamideHCID 6228—
생성물5-(2-Methylpropyl)-8-[3-(trifluoromethyl)phenyl]-3H,6H-1,4,5a,8a-tetraazaacenaphthylen-3-oneHCID 15702784—

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온도0 °C

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To a solution of 500 mg of 4,5-dihydro-5-thioxo-8-[3-(trifluoromethyl)phenyl]-3H,6H-1,4,5a,8a-tetraazaacenaphthylen-3-one (prepared as described in Example 8) in 10.0 ml of N,N-dimethylformamide was added 1.5 ml of 1N sodium hydroxide. The reaction mixture was cooled to 0° C. in an ice bath, then 0.5 ml of 30% hydrogen peroxide was added to the mixture dropwise. The reaction mixture was stirred at 0° C. for 30 minutes, then 1.0 ml of isobutylamine was added in one portion and the mixture was allowed to warm to room temperature, then was stirred for 2 hours. The solid was collected by filtration and washed with water, then ether to give 223 mg of the product of the example as a white solid, m.p. 266°-268° C. Following the procedure of Example 14 and reacting, 4,5-dihydro-5-thioxo-8-[3-(trifluoromethyl)phenyl]3H ,6H-1,4,5a,8a-tetraazaacenaphthylen-3-one with the appropriate primary aliphatic amine or cyclic secondary amine, the products of Examples 15-27 were obtained as set forth in Table III.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04916137
출처 데이터셋uspto-grants-1990_04
ORD IDord-f71a7546a89e403c9615866a626c22af
출처 메모uspto-grants-1990_04