Hydrochloric Acid → HCID 73472949, compound
Reaction equation
[CH:1](=[C:5]1[S:9][C:8](=[O:10])[N:7]([CH2:11][S:12][C:13]2[N:18]3[CH:19]=[CH:20][N:21]=[C:17]3[CH:16]=[CH:15][CH:14]=2)[C:6]1=[O:22])[CH2:2][CH2:3][CH3:4].[ClH:23]>CO>[ClH:23].[CH:1](=[C:5]1[S:9][C:8](=[O:10])[N:7]([CH2:11][S:12][C:13]2[N:18]3[CH:19]=[CH:20][N:21]=[C:17]3[CH:16]=[CH:15][CH:14]=2)[C:6]1=[O:22])[CH2:2][CH2:3][CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1.26 g (3.78 mmol) of 5-butylidene-3-(imidazo[1,2-a]pyridin-5-ylthio)methylthiazolidine-2,4-dione in 30 ml of methanol, 0.5 ml of concentrated hydrochloric acid was added. After the solvent was distilled off, the residue was washed with diethyl ether to yield 1.33 g (100%, light yellow solid) of the desired product.
Workup
- distillationAfter the solvent was distilled off
- washthe residue was washed with diethyl ether
Sources & evidence
- ORD record
- ord-ea4645bd874f439d96f1c069e204e728
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05840732
Reaction notes
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