Hydrochloric Acid → HCID 86745684, compound
Reaction equation
C([O:5][C:6]([CH2:8][O:9][N:10]=[C:11]1[C:20]2[C:15](=[C:16]([CH3:24])[C:17]([CH3:23])=[C:18]([OH:22])[C:19]=2[CH3:21])[O:14][C:13]([CH2:26][O:27][C:28]2[CH:41]=[CH:40][C:31]([CH2:32][CH:33]3[S:37][C:36](=[O:38])[NH:35][C:34]3=[O:39])=[CH:30][CH:29]=2)([CH3:25])[CH2:12]1)=[O:7])(C)(C)C.Cl>O1CCOCC1>[C:6]([CH2:8][O:9][N:10]=[C:11]1[C:20]2[C:15](=[C:16]([CH3:24])[C:17]([CH3:23])=[C:18]([OH:22])[C:19]=2[CH3:21])[O:14][C:13]([CH2:26][O:27][C:28]2[CH:41]=[CH:40][C:31]([CH2:32][CH:33]3[S:37][C:36](=[O:38])[NH:35][C:34]3=[O:39])=[CH:30][CH:29]=2)([CH3:25])[CH2:12]1)([OH:7])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 0.7 g of 5-[4-(4-t-butoxycarbonylmethoxyimino-6-hydroxy-2,5,7,8-tetramethylchroman -2ylmethoxy)benzyl]thiazolidine-2,4-dione (prepared as described in Example 26) and 7 ml of a 4N dioxane solution of hydrogen chloride was allowed to stand at room temperature for 15 hours. At the end of this time, the solvent was distilled off and the residue was washed with warm water to give the title compound, softening at 75°-85° C.
Workup
- distillationAt the end of this time, the solvent was distilled off
- washthe residue was washed with warm water
Sources & evidence
- ORD record
- ord-0e105bd4ed8348fcb3c2c80f1dffdad9
- Source dataset
- uspto-grants-1992_04
- Patent number
- US05104888
Reaction notes
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