Hydrochloric Acid → HCID 73472899, compound
Reaction equation
[CH:1](=[C:5]1[S:9][C:8](=[O:10])[N:7]([CH2:11][CH2:12][CH2:13][CH2:14][S:15][C:16]2[N:21]3[C:22]([C:25](=[O:30])[C:26]([F:29])([F:28])[F:27])=[CH:23][N:24]=[C:20]3[CH:19]=[CH:18][CH:17]=2)[C:6]1=[O:31])[CH2:2][CH2:3][CH3:4].[ClH:32]>CO>[ClH:32].[CH:1](=[C:5]1[S:9][C:8](=[O:10])[N:7]([CH2:11][CH2:12][CH2:13][CH2:14][S:15][C:16]2[N:21]3[C:22]([C:25](=[O:30])[C:26]([F:29])([F:28])[F:27])=[CH:23][N:24]=[C:20]3[CH:19]=[CH:18][CH:17]=2)[C:6]1=[O:31])[CH2:2][CH2:3][CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 200 mg (0.42 mmol) of 5-butylidene-3-[4-(3-trifluoroacetylimidazo[1,2-a]pyridin-5-ylthio)butyl]-thiazolidine-2,4-dione in 5 ml of methanol, 0.1 ml of concentrated hydrochloric acid was added. After the solvent was distilled off, the residue was washed with diethyl ether to yield 220 mg (100%, yellow oily substance) of the desired product.
Workup
- distillationAfter the solvent was distilled off
- washthe residue was washed with diethyl ether
Sources & evidence
- ORD record
- ord-4e08d02027e7440e8533d58ce6391fe8
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05840732
Reaction notes
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