Methanol → 4-Methoxy-1H-pyrrolo[2,3-b]pyridine
Reaction equation
Cl[C:2]1[CH:10]=[CH:9][N:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2.[OH-:11].[Na+].[CH3:13]O>>[CH3:13][O:11][C:2]1[CH:10]=[CH:9][N:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2Participants
4
Procedure
4-methoxy-7-azaindole 20 was prepared by reacting 4-chloro-7-azaindole 24 (prepared as described in Example 9) with sodium hydroxide in methanol as described by Girgis, N. et.al., J. Heterocyclic. Chem. 1989, 26:317-325.
Sources & evidence
- ORD record
- ord-dc18b7b764d643889a20c35361603542
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07893075B2
Reaction notes
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