Hydrochloric Acid → HCID 21275442, compound
Reaction equation
[ClH:1].Cl.C([N:10]1[CH2:29][CH2:28][C:13]2([C:17](=[O:18])[N:16]([O:19]CC3C=CC=CC=3)[C:15](=[O:27])[CH2:14]2)[CH2:12][CH2:11]1)C1C=CC=CC=1>[Pd].CO>[ClH:1].[OH:19][N:16]1[C:15](=[O:27])[CH2:14][C:13]2([CH2:12][CH2:11][NH:10][CH2:29][CH2:28]2)[C:17]1=[O:18]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
In a mixture solvent consisting of methanol (100 ml) and 1N hydrochloric acid (50 ml) was dissolved 8-benzyl-2-benzyloxy-2,8-diazaspiro[4,5]decane-1,3-dione hydrochloride (16.0 g). The solution was subjected to catalytic reduction at 40° C. for 12 hours under atmospheric pressure, using palladium as the catalyst. After the reaction, the catalyst was removed, and the solvent was evaporated off under reduced pressure. The residual solid was recrystallized from ethanol to obtain 8.9 g of a colorless solid, m.p. 250° to 277° C.
Workup
- customAfter the reaction
- customthe catalyst was removed
- customthe solvent was evaporated off under reduced pressure
- customThe residual solid was recrystallized from ethanol
Sources & evidence
- ORD record
- ord-440df8b502784df39e5cfedddaa105a7
- Source dataset
- uspto-grants-1989_02
- Patent number
- US04804665
Reaction notes
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