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Chloroacetonitrile → 3-Cyanomethyl-2,3-dihydro-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole

HRID 1489511
ノート
印刷プレビュー

反応式

HRID 1489511 の反応式
[H-].[Na+].[CH3:3][C:4]1[NH:5][C:6](=[O:17])[N:7]([N:9]=[CH:10][C:11]2[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=2)[CH:8]=1.Cl[CH2:19][C:20]#[N:21]>CN(C)C=O>[C:20]([CH2:19][N:5]1[C:4]([CH3:3])=[CH:8][N:7]([N:9]=[CH:10][C:11]2[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=2)[C:6]1=[O:17])#[N:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7856ChloroacetonitrileHCID 24758Sodium hydrideHCID 541240302,3-Dihydro4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole

生成物 1

HCID 867514133-Cyanomethyl-2,3-dihydro-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

0.72 g of sodium hydride are added to a suspension of 4.1 g of 2,3-dihydro-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole in 80 ml of N,N-dimethylformamide. The mixture is heated to 50°, treated with a solution of 1.89 g of chloroacetonitrile in 20 ml of N,N-dimethylformamide, and stirred for 30 minutes. The N,N-dimethylformamide is then removed on a rotary evaporator. In a mixer, the residue is mixed intimately with water. The crystals are filtered off, yielding the title compound melting at 195°-198°.

後処理

  1. temperatureThe mixture is heated to 50°
  2. customThe N,N-dimethylformamide is then removed on a rotary evaporator
  3. additionIn a mixer, the residue is mixed intimately with water
  4. filtrationThe crystals are filtered off

出典と根拠

ORDレコード
ord-7d31497fca674e108d78873ec29a352a
出典データセット
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05679623

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート