| Identification | More | [Name]
N-(2,6-Diphenylmethyl)-1-piperazine acetylamine | [CAS]
5294-61-1 | [Synonyms]
1-[(2,6-DIMETHYLANILINO)CARBONYL-METHYL]-PIPERAZINE
N-(2,6-DIMETHYLPHENYL)-1-PIPERAZIN-ACETAMIDE
N-(2,6-DIMETHYLPHENYL)-1-PIPERAZINEACETAMIDE
N-(2,6-DIMETHYL-PHENYL)-2-PIPERAZIN-1-YL-ACETAMIDE
N-(2,6-Diphenylmethyl)-1-piperazine acetylamine
1-[N-(2,6-dimethylphenyl)carbamoylmethyl]piperazine
RZ-2
1-(2,6-Dimethylphenyl)-1-Piperazineacetamide
N-(2,6-Dimethylphenyl)-1-Piper
N-(2,6-Dimethylphenyl)-2-1-Piperazinyl)Acetamide
1-Piperazineaceto-2',6'-xylidide
4-[(2,6-Dimethylphenyl)aminocarbonylmethyl]piperazine
N-(2,6-Dimethylphenyl)-2-piperazinylacetamide
RS 94287 | [EINECS(EC#)]
610-916-8 | [Molecular Formula]
C14H21N3O | [MDL Number]
MFCD06384973 | [Molecular Weight]
247.34 | [MOL File]
5294-61-1.mol |
| Chemical Properties | Back Directory | [Appearance]
Pale Beige Solid | [Melting point ]
110-112°C | [Boiling point ]
411.2±45.0 °C(Predicted) | [density ]
1.101±0.06 g/cm3(Predicted) | [vapor pressure ]
0-0Pa at 20-25℃ | [storage temp. ]
-20°C Freezer | [solubility ]
DMSO, Methanol | [form ]
Crystalline Powder | [pka]
14.62±0.70(Predicted) | [color ]
Light gray | [Usage]
A metabolite of Ranolazine | [InChIKey]
NJKRFQIWDJSYOK-UHFFFAOYSA-N | [LogP]
0.74 at 20℃ and pH12 | [CAS DataBase Reference]
5294-61-1(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
Pale Beige Solid | [Uses]
A metabolite of Ranolazine | [Uses]
A metabolite of Ranolazine. | [Synthesis]
The general procedure for the synthesis of N-(2,6-dimethylphenyl)-1-piperazine acetamide from piperazine hexahydrate and 2,6-dimethylchloroacetanilide was as follows: 58.3 g (0.3 mol) of piperazine hexahydrate was dissolved in 230 ml of ethanol, followed by the addition of 50.0 g (0.25 mol) of 2-chloro-N-(2,6-dimethylphenyl)acetamide. The reaction mixture was heated under reflux conditions for 3 hours until the reaction was complete. After completion of the reaction, the mixture was cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure followed by addition of 80 ml of water. The mixture was extracted with water and dichloromethane, and after separation of the organic layer, it was concentrated under vacuum at 60 °C to give 39.4 g of N-(2,6-dimethylphenyl)-1-piperazine acetamide in 63% yield. The product was characterized by 1HNMR (CDCl3): δ 2.23-2.27 (s, 6H), 2.67 (s, 4H), 2.96-2.98 (t, 4H), 3.19-3.21 (s, 2H), 7.08-7.26 (m, 3H), 8.69 (s, 1H). | [References]
[1] Patent: US2013/90475, 2013, A1. Location in patent: Paragraph 0029; 0030 |
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