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

HRID 1731916
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인쇄 미리보기

반응식

HRID 1731916 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.).

후처리

  1. temperatureThe 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-05247bf387974272aa0db41804ac250d
    출처 데이터셋
    uspto-grants-1986_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04623725

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