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(3-Methylpyridin-4-yl)methanamine → 1-[5-Methyl-2-(3-methyl-4-pyridinyl)-1H-imidazol-4-yl]ethanone

HRID 615329
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인쇄 미리보기

반응식

HRID 615329 반응식
[CH3:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8][NH2:9].[CH3:10][C:11](=[O:18])[C:12](=[N:16]O)[C:13](=O)[CH3:14]>C(#N)C>[CH3:14][C:13]1[NH:9][C:8]([C:7]2[CH:6]=[CH:5][N:4]=[CH:3][C:2]=2[CH3:1])=[N:16][C:12]=1[C:11](=[O:18])[CH3:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1514375(3-Methylpyridin-4-yl)methanamineHCID 178468373HCID 178468373, 화합물

생성물 1

HCID 133879411-[5-Methyl-2-(3-methyl-4-pyridinyl)-1H-imidazol-4-yl]ethanone수율 41%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
-10 °C

실험 절차

A mixture consisting of 7.1 g (0.058 mole) of 3-methyl-4-pyridylmethylamine, 6.25 g (0.051 mole) of 2,3,4-pentanetrione 3-oxime, and 125 ml of acetonitrile was stirred at the reflux temperature for five hours. After cooling at -10° C., a precipitate formed. This was collected, washed with a little cold acetonitrile, and dried. Recrystallization from a mixture of chloroform and hexane gave 4.5 g of the desired product, mp 185°-187° C.

후처리

  1. customa precipitate formed
  2. customThis was collected
  3. washwashed with a little cold acetonitrile
  4. customdried
  5. customRecrystallization
  6. additionfrom a mixture of chloroform and hexane

출처 및 근거

ORD 기록
ord-a13ef6c8be294949a5d20e9a4c964900
출처 데이터셋
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04499097

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