Hydrochloric Acid → 5-(3,4,5,6,7,8-hexahydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine dihydrochloride
Reaction equation
[CH2:1]1[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH2:4][CH2:3][N:2]1[CH2:11][C:12]1[C:13]([NH2:19])=[N:14][C:15]([CH3:18])=[N:16][CH:17]=1.[ClH:20]>C(O)C>[ClH:20].[ClH:20].[CH2:1]1[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH2:4][CH2:3][N:2]1[CH2:11][C:12]1[C:13]([NH2:19])=[N:14][C:15]([CH3:18])=[N:16][CH:17]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1.74 g (0.00673 mol) of 5-(3,4,5,6,7,8-hexahydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine in 40 ml of ethanol was treated with 3.85 ml (0.0135 mol) of 3.5N ethanolic hydrochloric acid. The solution was completely freed from the solvents and the residue was recrystallized from methanol/diethyl ether. 2.16 g (97%) of 5-(3,4,5,6,7,8-hexahydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine dihydrochloride were obtained as white crystals; m.p. 248°-250°.
Workup
- customthe residue was recrystallized from methanol/diethyl ether
Sources & evidence
- ORD record
- ord-fef790fa3f8a4d7cb96a6972e07ce034
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05688798
Reaction notes
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