Potassium Hydroxide → HCID 14390329, compound
Reaction equation
C([O:3][C:4](=[O:28])[CH2:5][CH2:6][CH2:7][NH:8][C:9](=[O:27])[CH2:10][N:11]1[C:15]2=[N:16][CH:17]=[CH:18][CH:19]=[C:14]2[N:13]=[C:12]1[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([Cl:26])[CH:21]=1)C.[OH-].[K+]>C(O)C>[OH2:3].[Cl:26][C:22]1[CH:21]=[C:20]([C:12]2[N:11]([CH2:10][C:9]([NH:8][CH2:7][CH2:6][CH2:5][C:4]([OH:28])=[O:3])=[O:27])[C:15]3=[N:16][CH:17]=[CH:18][CH:19]=[C:14]3[N:13]=2)[CH:25]=[CH:24][CH:23]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4-[[(2-(3chlorophenyl)-3H-imidazo[4,5-b]pyridine-3yl]acetyl]amino]butanoic acid ethyl ester (2.4 g, 0.006 mole) and potassium hydroxide (0.5 g) in 100 ml of ethanol was heated at reflux for 2 hrs. The reaction mixture was evaporated to dryness. The residue was dissolved in water, filtered, and the filtrate was acidified with acetic acid. The precipitate, which had formed, was collected by filtration, washed with water, and dried. The solid was recrystallized from ethanol-water, collected by filtration, washed with water, and dried under high vacuum at 78° C. over 2 days to give 0.93 g (42%), mp 207°-8° C.
Workup
- temperaturewas heated
- temperatureat reflux for 2 hrs
- customThe reaction mixture was evaporated to dryness
- dissolutionThe residue was dissolved in water
- filtrationfiltered
- customThe precipitate, which had formed
- filtrationwas collected by filtration
- washwashed with water
- customdried
- customThe solid was recrystallized from ethanol-water
- filtrationcollected by filtration
- washwashed with water
- customdried under high vacuum at 78° C. over 2 days
- customto give 0.93 g (42%), mp 207°-8° C.
Sources & evidence
- ORD record
- ord-829cd5c3a9fc4e7e936f1c0d0da95ff6
- Source dataset
- uspto-grants-1988_09
- Patent number
- US04772600
Reaction notes
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