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Acetic Acid → (3-bromo-2-methoxy-benzyl-4,5-dihydro-1H-imidazol-2-yl)-amine

HRID 561253
ノート
印刷プレビュー

反応式

HRID 561253 の反応式
C(O)(=O)C.[Br:5][C:6]1[C:7]([O:14][CH3:15])=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH2:9][NH2:10].CS[C:18]1[N:19](C(OC)=O)[CH2:20][CH2:21][N:22]=1>CO>[Br:5][C:6]1[C:7]([O:14][CH3:15])=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH2:9][N:10]1[CH2:21][CH2:20][N:19]=[C:18]1[NH2:22]
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 176Acetic AcidHCID 109429534,5-Dihydro-2-(methylthio)-1h-imidazole-1-carboxylic acid methyl esterHCID 57813384(3-Bromo-2-methoxyphenyl)methanamine

生成物 1

HCID 66725049(3-bromo-2-methoxy-benzyl-4,5-dihydro-1H-imidazol-2-yl)-amine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

10 mL of acetic acid (HOAc) was added to a solution of 3.9 g of 3-bromo-2-methoxy-benzylamine 8 and 3.1 g of methyl 2-(methylthio)-4,5-dihydro-1H-imidazole-1-carboxylate in 100 mL of methanol. The resulting solution was heated to a gentle reflux and refluxed overnight. The solution was cooled to room temperature, quenched with sodium hydroxide and extracted with ethyl acetate. The combined organic extracts were washed with brine and dried over magnesium sulfate. The mixture was then filtered. The solvents were removed under vacuum. The remaining residue was purified by chromatography on silica gel (10% saturated ammonia methanol in dichloromethane) to give (3-bromo-2-methoxy-benzyl-4,5-dihydro-1H-imidazol-2-yl)-amine 9.

後処理

  1. temperatureThe resulting solution was heated to
  2. temperaturea gentle reflux
  3. temperaturerefluxed overnight
  4. customquenched with sodium hydroxide
  5. extractionextracted with ethyl acetate
  6. washThe combined organic extracts were washed with brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationThe mixture was then filtered
  9. customThe solvents were removed under vacuum
  10. customThe remaining residue was purified by chromatography on silica gel (10% saturated ammonia methanol in dichloromethane)

出典と根拠

ORDレコード
ord-d38b29436c584aff9ebd74b3f02c8b6c
出典データセット
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08063231B2

反応ノート

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