1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one → HCID 21408224, compound
Reaction equation
Cl.[CH3:2][N:3]([CH2:5][CH:6]1[CH2:15][CH2:14][C:13]2[C:8](=[CH:9][C:10]([O:16][CH3:17])=[CH:11][CH:12]=2)[C:7]1=[O:18])[CH3:4].[C:19]1([N:25]2[C:29]3([CH2:34]CNC[CH2:30]3)[C:28](=[O:35])[NH:27][CH2:26]2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C(O)C>[C:19]1([N:25]2[C:29]3([CH2:30][CH2:2][N:3]([CH2:5][CH:6]4[CH2:15][CH2:14][C:13]5[C:8](=[CH:9][C:10]([O:16][CH3:17])=[CH:11][CH:12]=5)[C:7]4=[O:18])[CH2:4][CH2:34]3)[C:28](=[O:35])[NH:27][CH2:26]2)[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 15.0 g of 2-[(dimethylamino)methyl]-3,4-dihydro-7-methoxy-1(2H)-naphthalenone, hydrochloride (1:1), 13.0 g of 1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one, and 250 ml of absolute ethanol is heated on a steam bath until all solids dissolve. The resulting solution is stirred for 16 hours at room temperature under nitrogen. The resulting precipitates are collected and washed with additional absolute ethanol to give 16.7 g of the title compound.
Workup
- temperatureis heated on a steam bath until all solids
- dissolutiondissolve
- customThe resulting precipitates
- customare collected
- washwashed with additional absolute ethanol
Sources & evidence
- ORD record
- ord-2e77bbd0eeb746f0bba9378b67cc9d45
- Source dataset
- uspto-grants-1977_09
- Patent number
- US04051248
Reaction notes
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