Hydrochloric Acid → HCID 19966035, compound
Reaction equation
[N:1]1([CH2:6][CH2:7][CH2:8][O:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([S:17][CH3:18])[C:12]=2[NH:19][C:20](=[O:36])[CH2:21][CH:22]2[C:35]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[O:29][C:28]3[C:23]2=[CH:24][CH:25]=[CH:26][CH:27]=3)[CH:5]=[CH:4][N:3]=[CH:2]1.[ClH:37]>CO.C(Cl)Cl>[ClH:37].[N:1]1([CH2:6][CH2:7][CH2:8][O:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([S:17][CH3:18])[C:12]=2[NH:19][C:20](=[O:36])[CH2:21][CH:22]2[C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][C:28]=3[O:29][C:30]3[C:35]2=[CH:34][CH:33]=[CH:32][CH:31]=3)[CH:5]=[CH:4][N:3]=[CH:2]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
100 mg of N-{2-[3-(1-imidazolyl)propoxy]methyl-6-methylthiophenyl}-2-(9H-xanthen-9-yl)acetamide (prepared as described in Example 1) were dissolved in a mixture of methanol and methylene chloride. An excess of concentrated aqueous hydrochloric acid was added to the solution, and then the solvent was removed by distillation under reduced pressure. The resulting residue was dissolved in methanol, and diethyl ether was added to produce 85 mg of the title compound as crystals, melting at 175°-184° C.
Workup
- customthe solvent was removed by distillation under reduced pressure
- dissolutionThe resulting residue was dissolved in methanol
- additiondiethyl ether was added
Sources & evidence
- ORD record
- ord-bcd7db09aa0f4ccbab7eae47c55355d8
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05534529
Reaction notes
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