Ethanol → HCID 19701563, compound
Reaction equation
[CH2:1]([OH:3])[CH3:2].[C:4]([O:8]/[N:9]=[C:10](\[C:19]1[C:24]([CH2:25][O:26][CH3:27])=[CH:23][CH:22]=[CH:21][N:20]=1)/[C:11]1[CH:16]=[C:15]([Br:17])[CH:14]=[CH:13][C:12]=1[OH:18])([CH3:7])([CH3:6])[CH3:5]>C(O)CC>[C:4]([O:8]/[N:9]=[C:10](\[C:19]1[C:24]([CH2:25][O:26][CH3:27])=[CH:23][CH:22]=[CH:21][N:20]=1)/[C:11]1[CH:16]=[C:15]([Br:17])[CH:14]=[CH:13][C:12]=1[OH:18])([CH3:7])([CH3:6])[CH3:5].[Br:17][C:15]1[CH:14]=[CH:13][C:12]([OH:18])=[C:2]([CH:16]=1)[C:1]([C:19]1[C:24]([CH2:25][O:26][CH3:27])=[CH:23][CH:22]=[CH:21][N:20]=1)=[O:3]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
Using ethanol, in place of n-propanol in Example 17, (Z)-2-(5-bromo-2-hydroxybenzoyl)-3-methoxymethylpyridine O-t-butyloxime (60 mg) (Compound 180) was produced from 2-(5-bromo-2-hydroxybenzoyl)-3-methoxymethylpyridine (80 mg).
Sources & evidence
- ORD record
- ord-d476a2c9c955453898e53243da40c824
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05716971
Reaction notes
Loading…