Methanesulfonyl chloride → Phenol, 4-(1H-imidazo(4,5-b)pyridin-2-yl)-2-methoxy-, methanesulfonate (ester)
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:10]2[NH:11][C:12]3[C:13]([N:18]=2)=[N:14][CH:15]=[CH:16][CH:17]=3)[CH:6]=[CH:7][C:8]=1[OH:9].[CH3:19][S:20](Cl)(=[O:22])=[O:21]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:10]2[NH:11][C:12]3[C:13]([N:18]=2)=[N:14][CH:15]=[CH:16][CH:17]=3)[CH:6]=[CH:7][C:8]=1[O:9][S:20]([CH3:19])(=[O:22])=[O:21]Participants
3
Procedure
Prepared analogously to Example 1 from 2-(3'-methoxy-4'-hydroxy-phenyl)-imidazo[4,5-b]pyridine and methanesulfonic acid chloride.
Sources & evidence
- ORD record
- ord-93a6f4aeda2e4e29ab372359c9e4825a
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04582837
Reaction notes
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