Tetraethyltin → 4-Ethyl-7-hydroxy-2-phenyl-oxazolo[4,5-c]pyridine-6-carboxylic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[N:10]=[C:9](Br)[C:8]2[N:12]=[C:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[O:14][C:7]=2[C:6]=1[OH:21])=[O:4].[CH2:22]([Sn](CC)(CC)CC)[CH3:23]>>[CH3:1][O:2][C:3]([C:5]1[N:10]=[C:9]([CH2:22][CH3:23])[C:8]2[N:12]=[C:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[O:14][C:7]=2[C:6]=1[OH:21])=[O:4]Participants
3
Procedure
Prepared from 4-bromo-7-hydroxy-2-phenyl-oxazolo[4,5-c]pyridine-6-carboxylic acid methyl ester, example 3a, and tetraethyltin under conditions analogous to example 3b. MS: (+) m/z 299.1 (M+1).
Sources & evidence
- ORD record
- ord-498c23ec4298449c972e1116cc1ade53
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08269008B2
Reaction notes
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