2-Bromoethyl methyl ether → 5-Fluoro-3-(2-methoxyethyl)-3H-benzothiazol-2-ylideneamine
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]([NH2:10])=[N:7][C:6]=2[CH:11]=1.[CH3:12][O:13][CH2:14][CH2:15]Br>>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8](=[NH:10])[N:7]([CH2:15][CH2:14][O:13][CH3:12])[C:6]=2[CH:11]=1Participants
3
Procedure
Commercially available 5-fluoro-benzothiazol-2-ylamine and 2-bromoethyl methyl ether were processed as described for Example 46A to afford the title compound. MS (ESI+) m/z 227 (M+H)+.
Sources & evidence
- ORD record
- ord-5a8d92b3617b4b95ae2c52127a9d3f11
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07875639B2
Reaction notes
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