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2,6-Dimethylaniline → 3-Isoxazolecarboxamide, N-(2,6-dimethylphenyl)-5-ethyl-

HRID 345777
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인쇄 미리보기

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HRID 345777 반응식
[CH2:1]([C:3]1[O:7][N:6]=[C:5]([C:8]([OH:10])=O)[CH:4]=1)[CH3:2].C(C1NC=CN=1)(C1NC=CN=1)=O.[CH3:23][C:24]1[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[C:25]=1[NH2:26]>CN(C=O)C>[CH3:23][C:24]1[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[C:25]=1[NH:26][C:8]([C:5]1[CH:4]=[C:3]([CH2:1][CH3:2])[O:7][N:6]=1)=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 68962,6-DimethylanilineHCID 5250894Bis-(1H-imidazol-2-YL)-methanoneHCID 64838115-Ethyl-1,2-oxazole-3-carboxylic acid

생성물 1

HCID 30761703-Isoxazolecarboxamide, N-(2,6-dimethylphenyl)-5-ethyl-수율 73%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

5.1 g (0.04 mole) of 5-ethyl isoxazole 3-carboxylic acid are dissolved in 100 ml of DMF under nitrogen, 13 g (0.08 mole) of carbonyl diimidazole are added and the mixture is stirred for 2 h at room temperature. 9.7 g (0.08 mole) of 2,6-dimethyl aniline are added and the mixture is stirred again for 48 h. After removal of the precipitate formed by filtration and evaporation of the solvent, the residue is crystallized from petroleum ether. M.p.=82°. The yield is 73%.

후처리

  1. stirringthe mixture is stirred again for 48 h
  2. customAfter removal of the precipitate
  3. customformed by filtration and evaporation of the solvent
  4. customthe residue is crystallized from petroleum ether

출처 및 근거

ORD 기록
ord-a13ecd5d9bab466db49b7ae7b1e99f2d
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05059614

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