Imidazole → (S)-2-Phenyl-2-(1H-imidazol-1-yl)-1-aminoethane
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]=1Participants
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
- temperatureAfter cooling the reaction mixture
- customcan be used for the acylating step without further purification
- 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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