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

HRID 615325
ノート
印刷プレビュー

反応式

HRID 615325 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 297MethaneHCID 962WaterHCID 20427660(2-Chloro-6-methylpyridin-3-YL)methanamineHCID 178468373HCID 178468373、化合物

生成物 1

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

試薬・触媒・溶媒 1

HCID 6342Acetonitrile
溶媒

反応条件

温度
5 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-19991feeec2a4c3ca05fce67fea48d46
出典データセット
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04499097

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート