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Dimethylformamide → 104614-80-4

HRID 986497
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반응식

HRID 986497 반응식
C([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10]1[N:14]=[C:13]([C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=2)[NH:12][N:11]=1)(=O)N.C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C.[Pb+4].C[N:40](C)[CH:41]=[O:42]>>[Cl:21][C:18]1[CH:17]=[CH:16][C:15]([C:13]2[N:14]=[C:10]3[N:11]([C:41](=[O:42])[NH:40][C:4]4[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=43)[N:12]=2)=[CH:20][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 178418268HCID 178418268, 화합물HCID 178513625HCID 178513625, 화합물

생성물 1

HCID 135458592104614-80-4

실험 절차

Seven grams of 3-(2-Carbamoylphenyl)-5-(4-chlorophenyl)-1H-1,2,4-triazole are dissolved in dry dimethylformamide (180 ml) at 50° C. Lead tetraacetate (10.4 g) is added under stirring and the reaction mixture is stirred under nitrogen for ten minutes. The reaction mixture is quenched in crushed ice (500 ml) containing concentrated hydrochloric acid (50 ml). The white solid which forms is collected, washed thoroughly with cold water and recrystallized from 2-methoxyethanol to afford 2-(4-chlorophenyl)-[1,2,4]-triazolo[1,5-c]quinazolin-5(6H)one, mp 315°-318°.

후처리

stirring
the reaction mixture is stirred under nitrogen for ten minutes
  • customThe reaction mixture is quenched in crushed ice (500 ml)
  • additioncontaining concentrated hydrochloric acid (50 ml)
  • customThe white solid which forms is collected
  • washwashed thoroughly with cold water
  • customrecrystallized from 2-methoxyethanol
  • 출처 및 근거

    ORD 기록
    ord-bc5206bdc97b45e1a0febccbe91e2d70
    출처 데이터셋
    uspto-grants-1987_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04713383

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