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N-(2,6-Diphenylmethyl)-1-piperazine acetylamine

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N-(2,6-Diphenylmethyl)-1-piperazine acetylamine manufacturers

  • CVT-2738
  • CVT-2738 pictures
  • $29.00
  • 2026-08-08
  • CAS:5294-61-1
  • Purity: 99.84%
  • Supply Ability: 10g
N-(2,6-Diphenylmethyl)-1-piperazine acetylamine Basic information
Product Name:N-(2,6-Diphenylmethyl)-1-piperazine acetylamine
Synonyms:N-(2,6-dimethylphenyl)-2-piperazin-1-yl-ethanamide;1-Piperazineacetamide, N-(2,6-dimethylphenyl)-;Ranolazine impurity G;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
CAS:5294-61-1
MF:C14H21N3O
MW:247.34
EINECS:610-916-8
Product Categories:Ranolazine;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;INTERMEDIATESOFRANOLAZINE
Mol File:5294-61-1.mol
N-(2,6-Diphenylmethyl)-1-piperazine acetylamine Structure
N-(2,6-Diphenylmethyl)-1-piperazine acetylamine Chemical Properties
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
pka14.62±0.70(Predicted)
form Crystalline Powder
color Light gray
Major Applicationpharmaceutical
InChI1S/C14H21N3O/c1-11-4-3-5-12(2)14(11)16-13(18)10-17-8-6-15-7-9-17/h3-5,15H,6-10H2,1-2H3,(H,16,18)/p+2
InChIKeyNJKRFQIWDJSYOK-UHFFFAOYSA-N
SMILES[N+H]2(CC[N+H2]CC2)CC(=O)Nc1c(cccc1C)C
LogP0.74 at 20℃ and pH12
CAS DataBase Reference5294-61-1(CAS DataBase Reference)
Safety Information
WGK Germany WGK 3
HazardClass IRRITANT
HS Code 2934990002
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Skin Sens. 1B
MSDS Information
N-(2,6-Diphenylmethyl)-1-piperazine acetylamine Usage And Synthesis
Chemical PropertiesPale Beige Solid
UsesA metabolite of Ranolazine.
Synthesis
PIPERAZINE HEXAHYDRATE

142-63-2

2-Chloro-N-(2,6-dimethylphenyl)acetamide

1131-01-7

N-(2,6-Diphenylmethyl)-1-piperazine acetylamine

5294-61-1

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
N-(2,6-Diphenylmethyl)-1-piperazine acetylamine Preparation Products And Raw materials
Raw materialsPiperazine-->Piperazine hexahydrate-->2-Chloro-N-(2,6-dimethylphenyl)acetamide
Preparation ProductsRanolazine
Tag:N-(2,6-Diphenylmethyl)-1-piperazine acetylamine(5294-61-1) Related Product Information
Thioacetamide 2',6'-Pipecoloxylidide Bensulfuron methyl Acetamide Acetaminophen Piperazine Kresoxim-methyl Methyl acrylate Chlorodimethylphenylsilane Methylparaben N-(2,6-Dimethylphenyl)-2-picolinamide N-(2,4,6-Trichlorophenyl)maleimide N,N-Dimethylacetamide Carbonyl sulfide Pyrazophos Methyl Parathion-methyl Methyl bromide