Hydrogen chloride-ethyl acetate → HCID 73472917, compound
Reaction equation
[CH:1](=[C:9]1[S:13][C:12](=[O:14])[N:11]([CH2:15][CH2:16][CH2:17][CH2:18][O:19][C:20]2[C:21]3[N:22]([CH:26]=[CH:27][N:28]=3)[CH:23]=[CH:24][CH:25]=2)[C:10]1=[O:29])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[ClH:30].C(OCC)(=O)C>CO>[ClH:30].[CH:1](=[C:9]1[S:13][C:12](=[O:14])[N:11]([CH2:15][CH2:16][CH2:17][CH2:18][O:19][C:20]2[C:21]3[N:22]([CH:26]=[CH:27][N:28]=3)[CH:23]=[CH:24][CH:25]=2)[C:10]1=[O:29])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a methanol solution of 2.03 g (4.9 mmol) of 5-octylidene-3-[4-(imidazo[1,2-a]pyridin-8-yloxy)butyl]thiazolidine-2,4-dione, 1.25 ml of 4N hydrochloric acid-ethyl acetate was added, followed by stirring. After the solvent was distilled off, the residue was washed with ether to yield 1.71 g (77.2%, white solid) of the desired product.
Workup
- distillationAfter the solvent was distilled off
- washthe residue was washed with ether
Sources & evidence
- ORD record
- ord-75849eb729e24be69f0f0c4cbc2b1df1
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05840732
Reaction notes
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