2-Bromoethyl methyl ether → 5-Tert-butyl-3-(2-methoxyethyl)thiazol-2(3h)-imine hydrobromide
Reaction equation
[C:1]([C:5]1[S:9][C:8]([NH2:10])=[N:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:11][O:12][CH2:13][CH2:14][Br:15]>>[BrH:15].[C:1]([C:5]1[S:9][C:8](=[NH:10])[N:7]([CH2:14][CH2:13][O:12][CH3:11])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
A mixture of Example 136A and commercially available 2-bromoethyl methyl ether (Aldrich) was processed using the method described in Example 46A to afford the title compound. MS (ESI+) m/z 215 (M+H)+.
Sources & evidence
- ORD record
- ord-6bae0336ba4e40509b106ce78b528d9d
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07875639B2
Reaction notes
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