HCID 54552716, compound → HCID 53977277, compound
Reaction equation
C([O:3][C:4]([C:6]([CH3:25])=[CH:7][C:8]1[CH:24]=[CH:23][C:11]([CH2:12][CH2:13][C:14]2[N:19]3[CH:20]=[N:21][CH:22]=[C:18]3[CH:17]=[CH:16][CH:15]=2)=[CH:10][CH:9]=1)=[O:5])C>[OH-].[Na+]>[C:4]([C:6]([CH3:25])=[CH:7][C:8]1[CH:24]=[CH:23][C:11]([CH2:12][CH2:13][C:14]2[N:19]3[CH:20]=[N:21][CH:22]=[C:18]3[CH:17]=[CH:16][CH:15]=2)=[CH:10][CH:9]=1)([OH:5])=[O:3]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
5-[p-(2-Ethoxycarbonylprop-1-enyl)phenethyl]imidazo[1,5-a]pyridine (0.33 g) in 10 ml of 0.5N sodium hydroxide is refluxed for 3 hours, cooled and extracted with ether. The aqueous phase is adjusted to pH=6 and the resulting solid is filtered off to yield 5-[p-(2-carboxyprop-1-enyl)phenethyl]imidazo[1,5-a]pyridine.
Workup
- temperaturecooled
- extractionextracted with ether
- filtrationthe resulting solid is filtered off
Sources & evidence
- ORD record
- ord-d7aad3f0b1514a8e8dd977eeb180f61c
- Source dataset
- uspto-grants-1986_05
- Patent number
- US04588732
Reaction notes
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