Hydrochloric Acid → HCID 66725663, compound
Reaction equation
[O:1]=[C:2]1[N:10]2[C:11]([CH2:14][NH:15]C(=O)OCC3C=CC=CC=3)=[N:12][N:13]=[C:9]2[N:8]([CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[C:7]2[N:6]=[CH:5][NH:4][C:3]1=2.[ClH:31]>CO.[Pd]>[ClH:31].[NH2:15][CH2:14][C:11]1[N:10]2[C:2](=[O:1])[C:3]3[NH:4][CH:5]=[N:6][C:7]=3[N:8]([CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[C:9]2=[N:13][N:12]=1Participants
5
Procedure
To the solution of benzyl [(5-oxo-9-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-3-yl)methyl]carbamate (0.30 g, 0.73 mmol) in methanol (20 mL) and 1 mL of conc. HCl was added 110% Pd/C under N2. The mixture was shaken under 30 PSI H2 for 3 hours. The reaction mixture was filtered through celite and concentrated to yield the desired product (210 mg, 92%). LCMS calculated for C12H18N7O(M+H): 276.2; found: 276.2.
Workup
- filtrationThe reaction mixture was filtered through celite and
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-509439a3ab9a4aa4a6828bf58a381a1e
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07511050B2
Reaction notes
Loading…