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Imidazole → 2-Amino-6-imidazolyl-3-nitropyridine

HRID 1974476
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인쇄 미리보기

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HRID 1974476 반응식
[NH2:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[C:4](Cl)[N:3]=1.[NH:12]1[CH:16]=[CH:15][N:14]=[CH:13]1.O>CN(C)C=O>[NH2:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[C:4]([C:13]2[NH:12][CH:16]=[CH:15][N:14]=2)[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 795ImidazoleHCID 962WaterHCID 27240356-Chloro-3-nitropyridin-2-ylamine

생성물 1

HCID 191015702-Amino-6-imidazolyl-3-nitropyridine수율 79.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
120 °C

실험 절차

In 80 ml of N,N-dimethylformamide were dissolved 4.00 g of 2-amino-6-chloro-3-nitropyridine and 15.69 g of imidazole, and the solution was stirred at 120° C. overnight. After spontaneous cooling to room temperature, 100 ml of water was added and the resulting crystals were collected by filtration. The crystals were rinsed with a small amount of water and dried under reduced pressure to provide 3.76 g of 2-amino-6-imidazolyl-3-nitropyridine. Physicochemical properties:

후처리

  1. temperatureAfter spontaneous cooling to room temperature
  2. filtrationthe resulting crystals were collected by filtration
  3. washThe crystals were rinsed with a small amount of water
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-8083c1e4eb534a719866e28c0fed96f7
출처 데이터셋
uspto-grants-1994_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05283244

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