Imidazole → 1-Phenylpyrazole
Reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH:8]1[CH:12]=[CH:11]N=C1.[C:13](#[N:15])C>>[C:2]1([N:8]2[CH:12]=[CH:11][CH:13]=[N:15]2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Procedure
Operating protocol A (82° C., 48 hours) was followed using 117 mg of Chxn-Py-Al (0.4 mmoles), 211 μl of bromobenzene (2 mmoles), 204 mg of imidazole (3 mmoles) and 1.2 ml of acetonitrile.
Workup
- customA (82° C., 48 hours)
Sources & evidence
- ORD record
- ord-fc48c0b25fa447c6ab1628cd8a372c6b
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07202367B2
Reaction notes
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