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2-(Methylamino)pyridine-3-methanol

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2-(Methylamino)pyridine-3-methanol Basic information

Product Name:
2-(Methylamino)pyridine-3-methanol
Synonyms:
  • [2-(Methylamino)-3-pyridyl]methanol
  • 2-(METHYLAMINO)-3-PYRIDINEMETHANOL 98%
  • 3-HYDROXYMETHYL 2-METHYLAMINO PYRIDINE
  • [2-(Methylamino)pyridin-3-yl]methanol
  • 2-(Methylamino)pyridine-3-methanol
  • 2-(N-Methylamino)-3-hydroxymethylpyridine
  • 2-(MethylaMino)-3-PyridineMethanol
  • 3-(Hydroxymethyl)-2-(methylamino)pyridine 98%
CAS:
32399-12-5
MF:
C7H10N2O
MW:
138.17
EINECS:
692-124-2
Product Categories:
  • Hydroxymethyl's
  • Pyridines
  • Heterocycle-Pyridine series
Mol File:
32399-12-5.mol
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2-(Methylamino)pyridine-3-methanol Chemical Properties

Boiling point:
312.2±32.0 °C(Predicted)
Density 
1.191±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
13.63±0.10(Predicted)
InChI
InChI=1S/C7H10N2O/c1-8-7-6(5-10)3-2-4-9-7/h2-4,10H,5H2,1H3,(H,8,9)
InChIKey
VYPMWCUNCNMNOM-UHFFFAOYSA-N
SMILES
C1(NC)=NC=CC=C1CO
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Safety Information

Safety Statements 
24/25
HS Code 
29333990
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2-(Methylamino)pyridine-3-methanol Usage And Synthesis

Description

2-(Methylamino)pyridine-3-methanol is an industrial chemical that is used as a solvent and in the production of potassium sulfate. It has a high boiling point, which makes it a good choice for large-scale industrial processes. 2-(Methylamino)pyridine-3-methanol is also an organic solvent, which can be used to dissolve many other molecules. 

Uses

2-(Methylamino)pyridine-3-methanol is a raw material for the synthesis of isavuconazolium sulfate (triazole antifungal drug).

Preparation

Method 1: 2-Chloronicotinic acid is used as the starting material, reacted with methylamine hydrochloride, potassium carbonate, and cuprous bromide in DMF solvent at 100°C to prepare 2-methylamino-3-pyridinecarboxylic acid, and then reduced with lithium aluminium hydride to obtain the target product 2-(Methylamino)pyridine-3-methanol.
Method 2: 2-Methylamino-3-pyridinecarboxylic acid tert-butyl ester is reduced to the 2-methylamino-3-pyridinemethanol in an organic solvent and the presence of sodium borohydride/Lewis acid or potassium borohydride/Lewis acid reducing agent. 180 mL of tetrahydrofuran, 11.4 g (0.300 mol) of potassium borohydride, and 20.5 g (0.150 mol) of zinc chloride are added to a 500 mL three-necked flask and stirred at room temperature for 2 hours. Add 25g (0.120mol) of tert-butyl 2-methylamino-3-pyridinecarboxylate and 84mL of toluene. During the addition process, bubbles are released, and the addition rate is controlled. Keep reflux until the addition and reaction are complete. Then cool to room temperature and add 20% sodium hydroxide solution until the solution is clear. Then add ethyl acetate 500mL*3 to extract three times, combine the organic phases, wash twice with saturated brine 250mL*2, dry with anhydrous sodium sulfate, and spin dry to obtain 2-methylamino-3-pyridinemethanol as a white solid. Then, recrystallize from isopropanol/n-hexane to obtain 13.0g of a white solid with a yield of 88.2%.

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