Hydrogen Bromide → HCID 71767645, compound
Reaction equation
C[O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][O:9][CH:10]2[C:13]2[NH:14][CH2:15][CH2:16][N:17]=2)=[C:5]([CH3:18])[CH:4]=1.[BrH:19]>>[BrH:19].[NH:17]1[CH2:16][CH2:15][N:14]=[C:13]1[CH:10]1[C:11]2[C:6](=[C:5]([CH3:18])[CH:4]=[C:3]([OH:2])[CH:12]=2)[CH2:7][CH2:8][O:9]1Participants
3
Procedure
2-(7-Methoxy-5-methylisochroman-1-yl)-4,5-dihydro-1H-imidazole (example 61, 100 mg) was dissolved in hydrobromic acid (1.5 mL, 47 w-% in water) and mixture was heated to reflux. After 5.5 hours mixture was cooled down to room temperature. Solvents were evaporated and the evaporation residue was triturated with ethanol to afford the title compound. (Yield 27 mg).
Workup
- temperaturemixture was heated to reflux
- customSolvents were evaporated
- customthe evaporation residue was triturated with ethanol
Sources & evidence
- ORD record
- ord-0265cf1f738140aa83c2d17745cc1d5e
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09249127B2
Reaction notes
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