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Hydrochloric Acid → 4-Chloro-1H-benzo[d]imidazol-5-amine

HRID 1157402
ノート
印刷プレビュー

反応式

HRID 1157402 の反応式
[Cl:1][C:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[CH:5]=[CH:4][C:3]=1[NH:11]C(=O)C.C(O)C.Cl>O>[Cl:1][C:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[CH:5]=[CH:4][C:3]=1[NH2:11]
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

5

反応物 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 4083933HCID 4083933、化合物

生成物 1

HCID 129684544-Chloro-1H-benzo[d]imidazol-5-amine

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
85 °C

実験手順

58 mg (0.277 mmol) of N-(4-chloro-1H-benzimidazol-5-yl)acetamide (24-1) was suspended in a mixture of water, ethanol and concentrated HCl (0.06:1:0.4) for a total of 1 mL. The suspension was stirred and heated at 85° C. under nitrogen for 1 hour and after this time everything was soluble. The heat was turned off the solution was stirred overnight. The reaction was quenched with saturated NaHCO3. The pH was adjusted to 8 by adding solid NaHCO3 and Na2CO3. Extracted the reaction with ethyl acetate, dried, filtered and evaporated to recover the desired product 24-2. MS (M+1): measured 168.2; theoretical 167.0. 1H NMR (CD3OD): 6.75 (dd, 1H), 7.37 (d, 1H), 7.93 (s, 1H).

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

後処理

  1. stirringwas stirred overnight
  2. customThe reaction was quenched with saturated NaHCO3
  3. additionby adding solid NaHCO3 and Na2CO3
  4. extractionExtracted
  5. customthe reaction with ethyl acetate
  6. customdried
  7. filtrationfiltered
  8. customevaporated
  9. customto recover the desired product 24-2

出典と根拠

ORDレコード
ord-50cae2dc47b24e4a85610be4e129b2d7
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07807684B2

反応ノート

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