Hydrochloric Acid → HCID 86753349, compound
Reaction equation
[C:1]([CH:6]=[C:7]1[S:11][C:10](=[O:12])[N:9]([CH2:13][CH2:14][CH2:15][CH2:16][S:17][C:18]2[N:23]3[CH:24]=[CH:25][N:26]=[C:22]3[CH:21]=[CH:20][CH:19]=2)[C:8]1=[O:27])([O:3][CH2:4][CH3:5])=[O:2].[ClH:28]>CO>[ClH:28].[C:1]([CH:6]=[C:7]1[S:11][C:10](=[O:12])[N:9]([CH2:13][CH2:14][CH2:15][CH2:16][S:17][C:18]2[N:23]3[CH:24]=[CH:25][N:26]=[C:22]3[CH:21]=[CH:20][CH:19]=2)[C:8]1=[O:27])([O:3][CH2:4][CH3:5])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 0.70 g (1.73 mmol) of 5-carboethoxymethylene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione in 20 ml of methanol, 0.20 ml of concentrated hydrochloric acid was added, followed by stirring, after which the solvent was distilled off. The residue was washed with diethyl ether to yield 0.74 g (96.8%, white solid) of the desired product.
Workup
- distillationafter which the solvent was distilled off
- washThe residue was washed with diethyl ether
Sources & evidence
- ORD record
- ord-2369fe53fef34bbeb5d1fcb2db1d9feb
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05840732
Reaction notes
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