2-Phenylimidazole → HCID 66700010, compound
Reaction equation
[CH3:1][C:2]1([CH3:13])[O:11][C:10]2[C:5](=[CH:6][N:7]=[CH:8][CH:9]=2)[CH:4]2[O:12][CH:3]12.[C:14]1([C:20]2[NH:21][CH:22]=[CH:23][N:24]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[CH3:1][C:2]1([CH3:13])[O:11][C:10]2[CH:9]=[CH:8][N:7]=[CH:6][C:5]=2[CH:4]([N:21]2[CH:22]=[CH:23][N:24]=[C:20]2[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:3]1[OH:12]Participants
3
Procedure
Following the procedure in Example 1, using (±)-2,2-dimethyl-1a,7b-dihydro-2H-1,3-dioxa-6-aza-cyclopropa[a]naphthalene and 2-phenyl-1H-imidazole as starting materials, the title compound was prepared as a pale yellow solid.
Sources & evidence
- ORD record
- ord-bd81b7a02fde4e8aac3d055528b69480
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812183B2
Reaction notes
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