HCID 53898827, compound → HCID 19702865, compound
Reaction equation
C[O:2][C:3]([C:5]1[C:10]([C:11]([C:13]2[CH:18]=[CH:17][C:16]3[O:19][CH2:20][O:21][C:15]=3[CH:14]=2)=[O:12])=[CH:9][CH:8]=[C:7]([CH2:22][O:23][CH2:24][O:25][CH2:26][CH2:27][Si:28]([CH3:31])([CH3:30])[CH3:29])[N:6]=1)=[O:4]>CO>[CH3:29][Si:28]([CH3:31])([CH3:30])[CH2:27][CH2:26][O:25][CH2:24][O:23][CH2:22][C:7]1[N:6]=[C:5]([C:3]([OH:4])=[O:2])[C:10]([C:11]([C:13]2[CH:18]=[CH:17][C:16]3[O:19][CH2:20][O:21][C:15]=3[CH:14]=2)=[O:12])=[CH:9][CH:8]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
6-(2-Trimethylsilylethoxymethoxymethyl)-3-(3,4-methylenedioxyphenylcarbonyl)pyridine-carboxylic acid methyl ester was subjected to alkaline hydrolysis in methanol to give 6-(2-trimethylsilylethoxymethoxymethyl)-3-(3,4-methylenedioxyphenylcarbonyl)pyridine-2-carboxylic acid.
Sources & evidence
- ORD record
- ord-3cb436e2b09d4049b1b41c494adc98d6
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05714479
Reaction notes
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