Hydrochloric Acid → HCID 68515566, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH2:9][O:10][CH3:11])[CH:6]=[C:5]([O:12][CH3:13])[C:4]=1[C:14]1[N:15]2[N:21]=[C:20]([O:22][CH3:23])[C:19]([N:24]([CH2:31][CH2:32][CH3:33])[CH:25]3[CH2:30][CH2:29][O:28][CH2:27][CH2:26]3)=[C:16]2[S:17][CH:18]=1.C(OCC)(=O)C.[ClH:40]>C(OCC)C>[ClH:40].[CH3:13][O:12][C:5]1[CH:6]=[C:7]([CH2:9][O:10][CH3:11])[CH:8]=[C:3]([O:2][CH3:1])[C:4]=1[C:14]1[N:15]2[N:21]=[C:20]([O:22][CH3:23])[C:19]([N:24]([CH2:31][CH2:32][CH3:33])[CH:25]3[CH2:30][CH2:29][O:28][CH2:27][CH2:26]3)=[C:16]2[S:17][CH:18]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a mixture of 3-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-6-methoxy-N-propyl-N-(tetrahydro-2H-pyran-4-yl)pyrazolo[5,1-b][1,3]thiazole-7-amine (6.98 mg) and ethyl acetate (0.5 mL) was added hydrochloric acid in diethyl ether (1M, 14.7 μL). The mixture was stirred at room temperature for 1.5 hours and the solvent was removed by blowing nitrogen stream and dried to obtain the title compound (7.84 mg).
Workup
- customthe solvent was removed
- customdried
Sources & evidence
- ORD record
- ord-dd154217b7544b28b7eb33fdae6906f0
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08431603B2
Reaction notes
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