Hydrochloric Acid → HCID 86656598, compound
Reaction equation
[CH3:1][N:2]([CH3:28])[CH2:3][CH2:4][CH2:5][C:6]([N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[C:13]([C:18]([NH:20][O:21]C3CCCCO3)=[O:19])[CH:14]=2)[CH2:9]1)=[O:7].[ClH:29]>CO>[ClH:29].[CH3:28][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][C:6]([N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[C:13]([C:18]([NH:20][OH:21])=[O:19])[CH:14]=2)[CH2:9]1)=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 35 mg 2-[4-(dimethylamino)butanoyl]-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide, 1 ml methanol and 1.5 ml 0.1N, aqueous HCl is stirred for 3 h at ambient temperature. Subsequently, the mixture is lyophilized. 40 mg of a colorless solid are obtained. MH+=306.1
Sources & evidence
- ORD record
- ord-e17d72856d2c494880bbaee67115c716
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08575193B2
Reaction notes
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