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(1-Methyl-4-piperidinyl)methanamine

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(1-Methyl-4-piperidinyl)methanamine manufacturers

(1-Methyl-4-piperidinyl)methanamine Basic information
Product Name:(1-Methyl-4-piperidinyl)methanamine
Synonyms:4-Aminomethyl-1-methylpiperidine ,97%;1-Methyl-4-piperidinemethanamine;(1-Methyl-4-piperidinyl)methaneamine;(1-Methyl pyperidin-4-yl)methyl amine;(1-methyl-4-piperidnyl)methanamine;(1-methyl-4-piperidinyl)methylamine;TIMTEC-BB SBB009719;(1-METHYL-4-PIPERIDINYL)METHANAMINE
CAS:7149-42-0
MF:C7H16N2
MW:128.22
EINECS:230-477-2
Product Categories:C5 to C9;Building Blocks;C5 to C7;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks;New Products for Chemical Synthesis;Piperidines;Aminomethyl's;Pyrans, Piperidines &Piperazines;Pyrans, Piperidines & Piperazines
Mol File:7149-42-0.mol
(1-Methyl-4-piperidinyl)methanamine Structure
(1-Methyl-4-piperidinyl)methanamine Chemical Properties
Melting point 0°C
Boiling point 80 °C
density 0.901±0.06 g/cm3(Predicted)
Fp 0°C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form liquid
pka10.13±0.29(Predicted)
color Pale yellow
InChIInChI=1S/C7H16N2/c1-9-4-2-7(6-8)3-5-9/h7H,2-6,8H2,1H3
InChIKeyAGTPSAZJSOQXHJ-UHFFFAOYSA-N
SMILESN1(C)CCC(CN)CC1
CAS DataBase Reference7149-42-0(CAS DataBase Reference)
Safety Information
Hazard Codes C,Xi
Risk Statements 34-20/22-22-10
Safety Statements 26-36/37/39-45-23
RIDADR 2735
WGK Germany 1
Hazard Note Corrosive
HazardClass IRRITANT
HS Code 29333990
Storage Class3 - Flammable liquids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Flam. Liq. 3
Skin Corr. 1C
MSDS Information
(1-Methyl-4-piperidinyl)methanamine Usage And Synthesis
Chemical PropertiesColourless liquid
Uses(1-methyl-4-piperidinyl)methanamine is a reagent used in the synthesis of novel indole-carboxamides which are inhibitors of neurotropic alphavirus.
Synthesis 1-Methylisonipecotamide (6.75g, 47. 5MMOLES) was dissolved in anhydrous THF (350mL), and the resulting mixture was added in portions to a stirred slurry of lithium aluminum hydride (1.8g, 47. 5mmoles) in anhydrous THF (100 mL) at 0 ℃ under nitrogen. The mixture was stirred at 0 ℃ for 30min and then heated at 66 ℃ for 25h under nitrogen. Distilled water (1.88 mL) was added dropwise to the stirred mixture at 0 ℃, followed by 20 percent aqueous sodium hydroxide (1.42 mL), and then distilled water (6.75mL), and the mixture was stirred for 15 min. The mixture was filtered, and the solids were washed with THF and dichloromethane. The combined filtrates were evaporated to dryness and chromatographed on a silica gel column (30x5 cm) using 15 percent-20 percent (10 percent CONC. ammonium hydroxide in METHANOL)-DICHLOROMETHANE as the eluant to give (1-Methyl-4-piperidinyl)methanamine (0.678g, 11percent).
References[1] Journal of Medicinal Chemistry, 2003, vol. 46, # 7, p. 1116 - 1119
[2] Patent: WO2004/22561, 2004, A1. Location in patent: Page 110-11
(1-Methyl-4-piperidinyl)methanamine Preparation Products And Raw materials
Raw materialsThionyl chloride-->Palladium-->Formaldehyde-->Nickel-->Isonipecotamide-->1-Methylpiperidine-4-carboxamide-->Tetrahydrofuran-->Lithium Aluminum Hydride
Tag:(1-Methyl-4-piperidinyl)methanamine(7149-42-0) Related Product Information
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