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Methyl iodide → HCID 20751408、化合物

HRID 2238631
ノート
印刷プレビュー

反応式

HRID 2238631 の反応式
CN(C)/[CH:3]=[CH:4]/[C:5]([C:7]1[N:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]2=[N:9][CH:8]=1)=O.[NH2:17][C:18]([NH2:20])=[S:19].[CH3:21][O-].[Na+].CI>C(O)CCC>[CH3:21][S:19][C:18]1[N:20]=[C:5]([C:7]2[N:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]3=[N:9][CH:8]=2)[CH:4]=[CH:3][N:17]=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 6328Methyl iodideHCID 2723790ThioureaHCID 10942334Sodium MethoxideHCID 59176797HCID 59176797、化合物

生成物 1

HCID 20751408HCID 20751408、化合物収率 64.7%

試薬・触媒・溶媒 1

HCID 2631-Butanol溶媒

反応条件

温度
85 °C

実験手順

1 g of (E)-3-(dimethylamino)-1-imidazo[1,2-a]pyridin-3-yl-2-propen-1-one [1-2] was dissolved in 10 mL of n-butanol, then 354 mg of thiourea and 377 mg of sodium methoxide were added, and the mixture was stirred at 85° C. for 2 hours. After cooling back to the room temperature, 868 μL of methyl iodide was added, and stirred at room temperature for 30 minutes. The solvent was distilled off until the volume is halved, the solid thus produced was taken and washed with diethyl ether and with water in the subsequent order, and then dried under reduced pressure to obtain 728 mg of 3-[2-methylthio-4-pyrimidinyl]imidazo[1,2-a]pyridine [1-3] as a grey solid.

後処理

  1. additionwas added
  2. stirringstirred at room temperature for 30 minutes
  3. distillationThe solvent was distilled off until the volume
  4. customthe solid thus produced
  5. washwashed with diethyl ether and with water in the subsequent order
  6. customdried under reduced pressure

出典と根拠

ORDレコード
ord-df210168c0fb47bfb2c8f3e98cc495e8
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07718801B2

反応ノート

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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