Ammonium Hydroxide → HCID 12298167, compound
Reaction equation
[C:1]([O:5][C:6](=[O:9])[CH2:7]C)(=[O:4])[CH2:2][CH3:3].[C:10]1([NH:16][C:17]2([C:30]([O:32][CH2:33][CH2:34][CH3:35])=[O:31])[CH2:22][CH2:21][N:20]([CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH2:19][CH2:18]2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[OH-:36].[NH4+]>>[C:6]([OH:5])(=[O:9])[C:7]([OH:31])=[O:36].[O:4]=[C:1]([N:16]([C:17]1([C:30]([O:32][CH2:33][CH2:34][CH3:35])=[O:31])[CH2:18][CH2:19][N:20]([CH2:23][C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=2)[CH2:21][CH2:22]1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH2:2][CH3:3]Participants
Procedure
260 parts of propanoic acid anhydride are added dropwise to 93 parts of propyl 4-(phenylamino)-1-(phenylmethyl)-4-piperidinecarboxylate while cooling in a water-bath. Upon completion, the whole is stirred and refluxed for 6 hours. After cooling, the reaction mixture is poured onto water, alkalized with ammonium hydroxide and the product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The residue is dissolved in petroleumether. The solution is filtered and the filtrate is evaporated. The oily residue is converted into the ethanedioate salt in 2-propanone. The salt is filtered off and crystallized from a mixture of 2-propanone and ethanol (10:1 by volume), yielding propyl 4-[N-(1-oxopropyl)-N-phenylamino]-1-(phenylmethyl)-4-piperidinecarboxylate ethanedioate; mp. 169.7° C.
Workup
- temperaturewhile cooling in a water-bath
- temperaturerefluxed for 6 hours
- temperatureAfter cooling
- additionthe reaction mixture is poured onto water
- extractionthe product is extracted with trichloromethane
- washThe extract is washed with water
- customdried
- filtrationfiltered
- customevaporated
- dissolutionThe residue is dissolved in petroleumether
- filtrationThe solution is filtered
- customthe filtrate is evaporated
- filtrationThe salt is filtered off
- customcrystallized from a mixture of 2-propanone and ethanol (10:1 by volume)
Sources & evidence
- ORD record
- ord-3985555385ba4ecf9c9eb1874a89aa4d
- Source dataset
- uspto-grants-1976_12
- Patent number
- US03998834
Reaction notes
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