Hydrochloric Acid → HCID 88008205, compound
Reaction equation
[CH3:1][N:2]1[C:6]2[CH:7]=[C:8]([O:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[N:18]3[CH2:23][CH2:22][O:21][CH2:20][CH2:19]3)[CH:9]=[CH:10][C:5]=2[N:4]=[C:3]1[CH2:24][O:25][C:26]1[CH:39]=[CH:38][C:29]([CH2:30][CH:31]2[S:35][C:34](=[O:36])[NH:33][C:32]2=[O:37])=[CH:28][CH:27]=1.[ClH:40]>O1CCOCC1>[ClH:40].[ClH:40].[CH3:1][N:2]1[C:6]2[CH:7]=[C:8]([O:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[N:18]3[CH2:23][CH2:22][O:21][CH2:20][CH2:19]3)[CH:9]=[CH:10][C:5]=2[N:4]=[C:3]1[CH2:24][O:25][C:26]1[CH:39]=[CH:38][C:29]([CH2:30][CH:31]2[S:35][C:34](=[O:36])[NH:33][C:32]2=[O:37])=[CH:28][CH:27]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.64 g of 5-{4-(1-methyl-6-[2-(morpholin-4-yl)phenoxy]-1H-benzimidazol-2-ylmethoxy)benzyl}thiazolidine-2,4-dione were dissolved in a mixture of 30 ml of concentrated hydrochloric acid and 30 ml of 1,4-dioxane. The resulting solution was stirred at room temperature for 90 minutes. The reaction mixture was evaporated to dryness, followed by the addition of ether. The insoluble product was collected by filtration and washed with ether, whereby 0.71 g of the title compound were obtained.
Workup
- customThe reaction mixture was evaporated to dryness
- additionfollowed by the addition of ether
- filtrationThe insoluble product was collected by filtration
- washwashed with ether
Sources & evidence
- ORD record
- ord-f4654361877b4d0ab95f83c05620dbac
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06432993B1
Reaction notes
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