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Hydrochloric Acid → 5,6-Dimethoxy-2-[5-methoxy-2-(2-pyridinyl)phenylthio]-1H-benzimidazole

HRID 1199462
ノート
印刷プレビュー

反応式

HRID 1199462 の反応式
[CH3:1][O:2][C:3]1[C:21]([O:22][CH3:23])=[CH:20][C:6]2[NH:7][C:8]([S:10][C:11]3[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:12]=3N)=[N:9][C:5]=2[CH:4]=1.Cl.N([O-])=O.[Na+].[N:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>O>[CH3:1][O:2][C:3]1[C:21]([O:22][CH3:23])=[CH:20][C:6]2[NH:7][C:8]([S:10][C:11]3[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:12]=3[C:30]3[CH:31]=[CH:32][CH:33]=[CH:34][N:29]=3)=[N:9][C:5]=2[CH:4]=1
参加物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 313Hydrochloric AcidHCID 1049PyridineHCID 198667012-[-5,6-Dimethoxy-2-1H-benzimidazolylthio]-4-methoxy benzenamineHCID 23668193Sodium Nitrite

生成物 1

HCID 198666535,6-Dimethoxy-2-[5-methoxy-2-(2-pyridinyl)phenylthio]-1H-benzimidazole

試薬・触媒・溶媒 1

HCID 962Water
溶媒
2 回

実験手順

The product of step (b) above (500 mg) was treated with concentrated hydrochloric acid (0.8 ml) and water (0.8 ml) to form a paste. The paste was stirred at 0°-10° and a solution of sodium nitrite (105 mg) in water (0.5 ml) added dropwise. After stirring for 40 minutes the resultant solution was added slowly to pyridine (5 ml) stirred at 80°. The mixture was stirred for a further 40 minutes then concentrated in vacuo. The residue was slurried with 0.880 ammonia and the mixture again concentrated in vacuo. The residue was slurried with water and extracted with ethyl acetate. The ethyl acetate was washed with water and brine, then dried and evaporated to leave a brown gum. Flash chromatography produced the required product as a pale brown solid, MS MW 393 bp 216.

後処理

  1. customto form a paste
  2. stirringstirred at 80°
  3. stirringThe mixture was stirred for a further 40 minutes
  4. concentrationthen concentrated in vacuo
  5. concentrationthe mixture again concentrated in vacuo
  6. extractionextracted with ethyl acetate
  7. washThe ethyl acetate was washed with water and brine
  8. customdried
  9. customevaporated
  10. customto leave a brown gum

出典と根拠

ORDレコード
ord-49e7dcebdfce42b28d01d0b452cb9002
出典データセット
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04900751

反応ノート

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