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Dimethylamine → 4-Dimethylamino-[1,2,4]triazolo[4,3-a]quinoxaline

HRID 1731934
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인쇄 미리보기

반응식

HRID 1731934 반응식
Cl[C:2]1[C:3]2[N:4]([CH:12]=[N:13][N:14]=2)[C:5]2[C:10]([N:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.[CH3:15][NH:16][CH3:17]>CN(C)C=O>[CH3:15][N:16]([CH3:17])[C:2]1[C:3]2[N:4]([CH:12]=[N:13][N:14]=2)[C:5]2[C:10]([N:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 674DimethylamineHCID 11261184-Chloro[1,2,4]triazolo[4,3-a]quinoxaline

생성물 1

HCID 66229934-Dimethylamino-[1,2,4]triazolo[4,3-a]quinoxaline수율 44%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A slurry of 2.0 g. (0.01 mole) of 4-chloro-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 2) in N,N-dimethylformamide (30 ml.) was saturated with dimethylamine gas and stirred at room temperature overnight. The mixture was poured over ice and the precipitate was removed by filtration. Recrystallization from ethanol gave 640 mg. (44% yield) of 4-dimethylamino-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 184°-186° C.

후처리

  1. additionThe mixture was poured over ice
  2. customthe precipitate was removed by filtration
  3. customRecrystallization from ethanol
  4. customgave 640 mg

출처 및 근거

ORD 기록
ord-203e7ba4c598406e9ac4a82047dfcbf9
출처 데이터셋
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04623725

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