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Methyl iodide → 6-Chloro-5-iodo-2-(methylthio)-1H-benzo[d]imidazole

HRID 340766
ノート
印刷プレビュー

反応式

HRID 340766 の反応式
C([O-])([O-])=O.[K+].[K+].I[CH3:8].[Cl:9][C:10]1[C:19]([I:20])=[CH:18][C:13]2[NH:14][C:15](=[S:17])[NH:16][C:12]=2[CH:11]=1>CC(C)=O>[Cl:9][C:10]1[C:19]([I:20])=[CH:18][C:13]2[N:14]=[C:15]([S:17][CH3:8])[NH:16][C:12]=2[CH:11]=1
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 6328Methyl iodide2 回HCID 11430Potassium Carbonate2 回HCID 574814685-Chloro-6-iodo-1H-benzo[d]imidazole-2(3H)-thione

生成物 1

HCID 574814886-Chloro-5-iodo-2-(methylthio)-1H-benzo[d]imidazole

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

K2CO3 (0.22 g, 1.61 mmol), followed by iodomethane (0.1 mL, 1.61 mmol), was added to a solution of 5-chloro-6-iodo-1,3-dihydro-2H-benzimidazole-2-thione (1 g, 3.22 mmol) in acetone (20 mL) at 0° C. The reaction was stirred at rt for 1 h. Additional K2CO3 (1.61 mmol) and iodomethane (1.61 mmol) were added. The reaction was stirred at rt overnight, then the volatiles were removed and the residue was partitioned between EtOAc and water. Concentration of the EtOAc layer afforded the desired product as a white foam, which was used in the next step without further purification.

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

後処理

  1. stirringThe reaction was stirred at rt overnight
  2. customthe volatiles were removed
  3. customthe residue was partitioned between EtOAc and water

出典と根拠

ORDレコード
ord-813520244f8f4eb3825465972b17b708
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895596B2

反応ノート

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