Imidazole → 3-(4-Methyl-1H-imidazol-1-yl)propan-1-amine
Reaction equation
N1C=CN=C1.CC1N(CCCN)C=CN=1.C(C1N(CCCN)C=CN=1)C.C[C:28]1[N:29]([CH2:34][CH2:35][CH2:36][NH2:37])[CH:30]=[C:31]([CH3:33])[N:32]=1.C1(C2N(CCCN)C=CN=2)C=CC=CC=1.C1(C2N=CN(CCCN)C=2)C=CC=CC=1>>[CH3:33][C:31]1[N:32]=[CH:28][N:29]([CH2:34][CH2:35][CH2:36][NH2:37])[CH:30]=1Participants
7
Reactant 6
Product 1
Procedure
By substituting the appropriate imidazole starting material in the above procedure, the following intermediates were prepared: 2-methyl-1H-imidazole-1-propanamine; 2-ethyl-1H-imidazole-1-propanamine; 2,4-dimethyl-1H-imidazole-1-propanamine; 2-phenyl-1H-imidazole-1-propanamine; and 4-phenyl-1H-imidazole-1-propanamine.
Workup
- customthe following intermediates were prepared
Sources & evidence
- ORD record
- ord-d0e2f899fc764fea92c01ad6dca769d1
- Source dataset
- uspto-grants-1985_11
- Patent number
- US04555519
Reaction notes
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