4-Methyloxybenzyl chloride → 1-(2-Thiazolylmethyl)-2,2'-bi-1H-imidazole
Reaction equation
Br[CH2:2][C:3]1[S:4][CH:5]=[CH:6][N:7]=1.COC1C=CC(CCl)=CC=1.[NH:18]1[CH:22]=[CH:21][N:20]=[C:19]1[C:23]1[NH:24][CH:25]=[CH:26][N:27]=1>>[S:4]1[CH:5]=[CH:6][N:7]=[C:3]1[CH2:2][N:18]1[CH:22]=[CH:21][N:20]=[C:19]1[C:23]1[NH:27][CH:26]=[CH:25][N:24]=1Participants
4
Procedure
If the procedure of Example 1 is repeated using 2- bromomethylthiazole rather than 4-methoxybenzyl chloride of Example 1, the products obtained are title compounds (7) and (8).
Workup
- customthe products obtained
Sources & evidence
- ORD record
- ord-f8ab6f42d6484d42a4952ca3bb945fe9
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04929744
Reaction notes
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