Imidazole → (S)-2-Phenyl-2-(1H-imidazol-1-yl)-1-aminoethane

HRID 54517Notes

Reaction equation

HRID 54517 reaction equation
[C:1]1([C@@H:7]2[CH2:9][NH:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH:10]1[CH:14]=[CH:13][N:12]=[CH:11]1>>[C:1]1([C@H:7]([N:10]2[CH:14]=[CH:13][N:12]=[CH:11]2)[CH2:9][NH2:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

3

Procedure

1 g of (R)(-)-2-phenyl-aziridine and 1.14 g of imidazole are heated at 120° for 24 hours. After cooling the reaction mixture can be used for the acylating step without further purification. An analytical sample can be obtained by chromatography over silica gel;

Workup

  1. temperatureAfter cooling the reaction mixture
  2. customcan be used for the acylating step without further purification
  3. customAn analytical sample can be obtained by chromatography over silica gel

Sources & evidence

ORD record
ord-ac94eab7979440e8ae1d0bd0f8ff29ec
Source dataset
uspto-grants-1997_04
Patent number
US05622982

Reaction notes

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