Ethyl Bromide → 1H-Imidazole, 1-ethyl-2-(6-methoxy-2-benzofuranyl)-, monohydrochloride
Reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:17]=[CH:16][C:7]2[CH:8]=[C:9]([C:11]3[NH:12][CH:13]=[CH:14][N:15]=3)[O:10][C:6]=2[CH:5]=1.[CH2:18](Br)[CH3:19]>>[ClH:1].[CH2:18]([N:12]1[CH:13]=[CH:14][N:15]=[C:11]1[C:9]1[O:10][C:6]2[CH:5]=[C:4]([O:3][CH3:2])[CH:17]=[CH:16][C:7]=2[CH:8]=1)[CH3:19]Participants
3
Procedure
This was prepared from 2-(6-methoxybenzofuran-2-yl) imidazole hydrochloride and ethyl bromide according to the procedure of example 2; m.p.=259°-261 ° C.
Sources & evidence
- ORD record
- ord-c5b3ffc2e45743b49e792b108453ea17
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05354769
Reaction notes
Loading…