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Methane → 1-[2-(2-Chloro-6-methyl-3-pyridinyl)-5-methyl-1H-imidazol-4-yl]ethanone

HRID 615325
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인쇄 미리보기

반응식

HRID 615325 반응식
[CH3:1][C:2](=O)[C:3](=[N:7]O)[C:4](=[O:6])[CH3:5].[Cl:10][C:11]1[C:16]([CH2:17][NH2:18])=[CH:15][CH:14]=[C:13]([CH3:19])[N:12]=1.O.C>C(#N)C>[Cl:10][C:11]1[C:16]([C:17]2[NH:18][C:2]([CH3:1])=[C:3]([C:4](=[O:6])[CH3:5])[N:7]=2)=[CH:15][CH:14]=[C:13]([CH3:19])[N:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 297MethaneHCID 962WaterHCID 20427660(2-Chloro-6-methylpyridin-3-YL)methanamineHCID 178468373HCID 178468373, 화합물

생성물 1

HCID 133879381-[2-(2-Chloro-6-methyl-3-pyridinyl)-5-methyl-1H-imidazol-4-yl]ethanone수율 18.5%

시약·촉매·용매 1

HCID 6342Acetonitrile
용매

반응 조건

온도
5 °C

실험 절차

A mixture of 0.7 g of 2,3,4-pentanetrione 3-oxime and 0.9 g of 2-chloro-6-methyl-3-pyridylmethylamine in 50 ml of acetonitrile was stirred at the reflux temperature for 4 hours. The reaction mixture was evaporated in vacuo to give an oil. The oil was boiled in 50 ml. of water, treated with activated charcoal and filtered. The filtrate was cooled at 5° C. to yield a precipitate. The precipitate was collected, washed with cold water and dried to give 0.25 g of the product of the Example as a white solid, mp 156°-158° C.

후처리

  1. customThe reaction mixture was evaporated in vacuo
  2. customto give an oil
  3. filtrationfiltered
  4. customto yield a precipitate
  5. customThe precipitate was collected
  6. washwashed with cold water
  7. customdried

출처 및 근거

ORD 기록
ord-19991feeec2a4c3ca05fce67fea48d46
출처 데이터셋
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04499097

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