2-Bromoethyl methyl ether → HCID 11608396, compound
Reaction equation
[Cl:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]2[C:10]([CH3:11])=[C:9]([CH3:12])[NH:8][C:7]=12.[CH3:13][O:14][CH2:15][CH2:16]Br>>[Cl:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]2[C:10]([CH3:11])=[C:9]([CH3:12])[N:8]([CH2:16][CH2:15][O:14][CH3:13])[C:7]=12Participants
3
Procedure
In accordance with the same procedures as in Step 2 of Example 198, except for using 7-chloro-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridine prepared in Step 1 of Example 198 and 2-bromoethyl methyl ether, the titled compound was obtained as a white solid. (Yield: 80%)
Sources & evidence
- ORD record
- ord-5111e1fc75734f6eb5f00994ca5b99d9
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188114B2
Reaction notes
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