4-(4-Methylpiperazino)benzylamine

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4-(4-Methylpiperazino)benzylamine Basic information
Product Name:4-(4-Methylpiperazino)benzylamine
Synonyms:4-(4-Methyl-1-piperazinyl)benzylamine;4-(4-Methylpiperazin-1-yl)benzylamine;BUTTPARK 98\50-54;ART-CHEM-BB B022037;AKOS B022037;4-(4-METHYLPIPERAZINO)BENZYLAMINE;4-(4-Methylpiperazin-1-yl)Benz;4-(4-Methylpiperazino)benzylam
CAS:216144-45-5
MF:C12H19N3
MW:205.3
EINECS:
Product Categories:Phenyls & Phenyl-Het;Piperazines;Piperazidine intermediates;Aminomethyl's;Phenyls & Phenyl-Het;Piperaizine
Mol File:216144-45-5.mol
4-(4-Methylpiperazino)benzylamine Structure
4-(4-Methylpiperazino)benzylamine Chemical Properties
Boiling point 122-124/0.05mm
density 1.065±0.06 g/cm3(Predicted)
storage temp. Store at Room Tem.
pka10.40±0.10(Predicted)
CAS DataBase Reference216144-45-5(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 36/37/38-34
Safety Statements 26-36/37/39-45
Hazard Note Corrosive
HS Code 2933599590
MSDS Information
4-(4-Methylpiperazino)benzylamine Usage And Synthesis
Synthesis
4-(4-METHYL-PIPERAZIN-1-YL)BENZONITRILE

34334-28-6

4-(4-Methylpiperazino)benzylamine

216144-45-5

General procedure for the synthesis of 4-(4-methyl-1-piperazinyl)benzylamine from 4-(4-methylpiperazin-1-yl)benzonitrile: Sodium borohydride (10 eq.) was added to a solution of 4-(4-methylpiperazin-1-yl)benzonitrile (1 eq.) and cobalt chloride hexahydrate (2.1 eq.). The reaction mixture was stirred for 5 hours and then filtered through a pad of diatomaceous earth. The organic phase was concentrated under reduced pressure. The yellow oil obtained was purified by rapid chromatography on silica gel (dichloromethane: methanol = 8:2) to afford the target compound 4-(4-methyl-1-piperazinyl)benzylamine as a white solid in 50% yield.1H NMR (400 MHz, methanol-d4): δ (ppm) 2.42 (s, 3H); 2.74 (t, J=8Hz, 4H); 3.17 (t. J=8Hz, 4H); 4.43 (s, 2H); 6.89 (d, J=8Hz, 2H); 7.18 (d, J=8Hz, 2H). Elemental analysis (C12H19N3) calculated values: C, 70.20; H, 9.33; N, 20.47; measured values: C, 70.10; H, 9.13; N, 20.27.

References[1] Tetrahedron Letters, 2013, vol. 54, # 38, p. 5204 - 5206
[2] Journal of Medicinal Chemistry, 2005, vol. 48, # 26, p. 8261 - 8269
[3] Journal of Medicinal Chemistry, 2014, vol. 57, # 12, p. 5293 - 5305
[4] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 7, p. 741 - 745
4-(4-Methylpiperazino)benzylamine Preparation Products And Raw materials
Raw materials4-(4-Methyl-piperazin-1-yl)benzonitrile
Tag:4-(4-Methylpiperazino)benzylamine(216144-45-5) Related Product Information
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