| Identification | Back Directory | [Name]
piritramide | [CAS]
302-41-0 | [Synonyms]
A 65
R 3365
Pirdolan
Dipidolor
Piridolan
Pirtramide
piritramide
Pirinitramide
DipiritraMide
Piritramide (1 mg/mL in Methanol)
Piritramide (1.0mg/ml in Acetonitrile)
1-[3-cyano-3,3-di(phenyl)propyl]-4-piperidino-isonipecotamide
[1,4'-Bipiperidine]-4'-carboxamide, 1'-(3-cyano-3,3-diphenylpropyl)-
1-[3-cyano-3,3-di(phenyl)propyl]-4-piperidin-1-ylpiperidine-4-carboxamide
1-[3-cyano-3,3-di(phenyl)propyl]-4-piperidin-1-yl-piperidine-4-carboxamide | [EINECS(EC#)]
206-124-3 | [Molecular Formula]
C27H34N4O | [MOL File]
302-41-0.mol | [Molecular Weight]
430.59 |
| Chemical Properties | Back Directory | [Melting point ]
149-150° | [Boiling point ]
544.82°C (rough estimate) | [density ]
1.0967 (rough estimate) | [refractive index ]
1.5900 (estimate) | [storage temp. ]
Controlled Substance, -20°C Freezer | [pka]
16.19±0.20(Predicted) |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White Low Melting Solid | [Originator]
Dipidolor ,Janssen W. ,Germany,1969 | [Uses]
Piritramide is a synthetic opioid commonly used in Germany and Austria for the analgesia of pediatric patients.
| [Definition]
ChEBI: Piritramide is a nitrile. | [Manufacturing Process]
A mixture of 84 parts of 3,3-diphenyl-3-cyanopropyl bromide, 41 parts of 4piperidino-4-piperidinecarboxamide, 64 parts of sodium carbonate, a small amount of potassium iodide and 1,200 parts of anhydrous toluene was stirred, and heated under reflux for 48 hours. At the end of this time the reaction mixture was allowed to cool to room temperature, and 500 parts of water were added. The resultant precipitate was removed by filtration, and triturated with diisopropyl ether. The crystalline material thus obtained was removed by filtration, and recrystallized from 320 parts of acetone, to give 1-(3,3diphenyl-3-cyanopropyl)-4-piperidino-4-piperidinecarboxamide, melting at about 149°C to 150°C. | [Therapeutic Function]
Analgesic |
|