Hydrochloric Acid → HCID 136378091, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([S:10]([N:13]2[CH2:18][CH2:17][N:16]([CH3:19])[CH2:15][CH2:14]2)(=[O:12])=[O:11])=[CH:6][C:5]=1[C:20]1[NH:25][C:24](=[O:26])[C:23]2=[C:27]([CH3:35])[N:28]=[C:29]([CH:30]3[CH2:34][CH2:33][CH2:32][CH2:31]3)[N:22]2[N:21]=1)[CH3:2].[ClH:36]>C(OCC)C>[ClH:36].[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([S:10]([N:13]2[CH2:18][CH2:17][NH:16][CH2:19][CH:14]2[CH3:15])(=[O:12])=[O:11])=[CH:6][C:5]=1[C:20]1[NH:25][C:24](=[O:26])[C:23]2=[C:27]([CH3:35])[N:28]=[C:29]([CH:30]3[CH2:31][CH2:32][CH2:33][CH2:34]3)[N:22]2[N:21]=1)[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
220 mg (0.42 mmol) of 2-[2-ethoxy-5-(4-methylpiperazine-1-sulphonyl)-phenyl]-5-methyl-7-cyclopentyl-3H-imidazo[5,-f][1,2,4]-triazin-4-one (Example 1) are suspended in 20 ml of diethyl ether and, after addition of 20 mg (0.462 mmol) of 1 molar ethereal HCl solution, stirred at room temperature for 30 minutes. The solvent is distilled off under reduced pressure and the residue is dried under high vacuum.
Workup
- distillationThe solvent is distilled off under reduced pressure
- customthe residue is dried under high vacuum
Sources & evidence
- ORD record
- ord-a68f4a8c18be455688c81eae76cd4018
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06476029B1
Reaction notes
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