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Ethyl orthoformate → 4,7-Dimethoxy-[1,2,4]triazolo[4,3-a]quinoxaline

HRID 2412884
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반응식

HRID 2412884 반응식
[CH3:1][O:2][C:3]1[C:4]([NH:15][NH2:16])=[N:5][C:6]2[C:11]([N:12]=1)=[CH:10][C:9]([O:13][CH3:14])=[CH:8][CH:7]=2.[CH2:17](OC(OCC)OCC)C>>[CH3:1][O:2][C:3]1[C:4]2[N:5]([CH:17]=[N:16][N:15]=2)[C:6]2[C:11]([N:12]=1)=[CH:10][C:9]([O:13][CH3:14])=[CH:8][CH:7]=2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 31214Ethyl orthoformateHCID 133856753,6-Dimethoxy-2-hydrazinoquinoxaline

생성물 1

HCID 133856924,7-Dimethoxy-[1,2,4]triazolo[4,3-a]quinoxaline

반응 조건

온도
100 °C

실험 절차

A mixture consisting of 1.5 g. (0.068 mole) of 3,6-dimethoxy-2-hydrazinoquinoxaline and 20 ml. of triethylorthoformate was heated with mechanical stirring in a preheated oil bath at 100° C. overnight (~16 hours). The resulting mixture was then cooled to room temperature, and the precipitate which formed was subsequently recovered by means of suction filtration and washed with ethanol to ultimately afford 1.8 g. of pure 4,7-dimethoxy-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 238°-240° C. (decomp.). Mass Spectrum: m/e, 230 (P); m/e, 231 (P+1); m/e, 232 (P+2).

후처리

temperature
The resulting mixture was then cooled to room temperature
  • customthe precipitate which formed
  • filtrationwas subsequently recovered by means of suction filtration
  • washwashed with ethanol to ultimately afford 1.8 g
  • 출처 및 근거

    ORD 기록
    ord-e515ae203fd4402abc4581d689e149ca
    출처 데이터셋
    uspto-grants-1985_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04495187

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