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Diethyl Oxalate → 1-cyclohexyl-6-trifluoromethyl-2,3(1H,4H)-quinoxalinedione

HRID 861458
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인쇄 미리보기

반응식

HRID 861458 반응식
[CH:1]1([NH:7][C:8]2[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][C:9]=2[NH2:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:19](OCC)(=[O:25])[C:20](OCC)=[O:21]>>[CH:1]1([N:7]2[C:8]3[C:9](=[CH:11][C:12]([C:15]([F:16])([F:17])[F:18])=[CH:13][CH:14]=3)[NH:10][C:20](=[O:21])[C:19]2=[O:25])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7268Diethyl OxalateHCID 24165451-N-cyclohexyl-4-(trifluoromethyl)benzene-1,2-diamine

생성물 1

HCID 220971991-cyclohexyl-6-trifluoromethyl-2,3(1H,4H)-quinoxalinedione

실험 절차

28 g (0.11 mol) of 2-cyclohexylamino-5-trifluoromethylaniline and 322 g (2.2 mol) of diethyl oxalate were refluxed for 2 hours. The reaction mixture was then concentrated, and the crude product was recrystallized from ethanol.

후처리

  1. concentrationThe reaction mixture was then concentrated
  2. customthe crude product was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-786e503dc11b480e8da3e4114a427d4c
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05714489

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