Hydrochloric Acid → N-Hydroxy-2-(pyridin-2-ylacetyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide hydrochloride
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][C:8]([N:10]1[CH2:19][CH2:18][C:17]2[C:12](=[CH:13][CH:14]=[C:15]([C:20]([NH:22][O:23]C3CCCCO3)=[O:21])[CH:16]=2)[CH2:11]1)=[O:9].[ClH:30]>O.CO>[ClH:30].[OH:23][NH:22][C:20]([C:15]1[CH:16]=[C:17]2[C:12](=[CH:13][CH:14]=1)[CH2:11][N:10]([C:8](=[O:9])[CH2:7][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=1)[CH2:19][CH2:18]2)=[O:21]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 75 mg 2-(pyridin-2-ylacetyl)-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide and 6 ml of a 0.1M solution of HCl in water in 4 ml methanol is stirred overnight at ambient temperature and evaporated. The mixture is dissolved in a mixture of 2 ml water and 2 ml acetonitrile and lyophilized. 75 mg of the title compound are obtained as colorless solid. MH+=312.1
Workup
- customevaporated
- dissolutionThe mixture is dissolved in a mixture of 2 ml water and 2 ml acetonitrile
Sources & evidence
- ORD record
- ord-bd2d9efed3324f2f9ebaeb57958f7ab3
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08575193B2
Reaction notes
Loading…