2,4-Dichloro-3-methylpyridine
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2,4-Dichloro-3-methylpyridine
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CAS No:
132097-09-7
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Formula:
C6H5Cl2N
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Chemical Name:
2,4-Dichloro-3-methylpyridine
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Synonyms:
2,4-Dichloro-3-methylpyridine;Pyridine, 2,4-dichloro-3-methyl-;2,4-Dichloro-3-picoline;2,4-dichloro-3-methyl-pyridine;PubChem5462;ACMC-1BY23;SCHEMBL542498;3-Methyl-2,4-dichloropyridine;CTK4B7724;DTXSID10611883
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CAS No:
Characteristics
12.9
2.8
1.319±0.06 g/cm3(Predicted)
218.7±35.0 °C(Predicted)
106.8±11.5 °C
1.547
0.183mmHg at 25°C
Safety Information
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
2,4-Dichloro-3-methylpyridine Use and Manufacturing
1.6 M n-Butyl lithium in hexanes (3.75 mL, 6.0 mmol) and anhydrous THF (5 mL) were added to a flame-dried flask under nitrogen atmosphere. This solution was cooled to-78C, 2, 4- Dichloro-pyridine was added dropwise while stirring and the mixture was stirred at-78C for 30 min after which time methyliodide (0.374 mL, 6.0 mmol) was added dropwise at-78C. This mixture was stirred at-78C for lh under nitrogen atmosphere after which time glacial ACOH (0.114 mL, 2.0 mmol) was added to give a reaction mixture pH (wet pH paper) of 5-6. The reaction mixture was dissolved in Et2O (100 mL), the organic layer was washed with water (10 mL), then brine (10 ML), dried with MGS04, and the solvent was evaporated in vacuo to give an oil which was purified by flash chromatography using HEXANES : CH2CL2 (50: 50 V/V) to hexanes: CH2CL2 : EtOAc (50: 47: 3 v/v/v) to give 2, 4-dichloro-3-methyl-pyridine as a white solid (589 mg, 72percent). It was noted that 2, 4-dichloro-3- methyl-pyridine readily sublimates in vacuo. 'H NMR (CD30D, 400 MHz) 8 8.15 (d, 1H), 7.46 (d, 1H), 2.50 (s, 3H). LRMS calculated for C6H5CL2N : 160.98, found: (MH) + 161.9.To a solution 2, 4-dichloro-3-methyrpyridine (2.0 g, 12.3 mmol) in anhydrous carbon tetrachloride (50 mL) was added recrystallized l-bromopyrrolidine-2, 5-dione (2.25 g, 12.6 mmol) and benzoyl benzenecarboperoxoate (400 mg, 1.6 mmol). The mixture was stirred at reflux for 2 hours. After cooling to room temperature, the solid material was removed by filtration and washed with carbon tetrachloride (2 x 10 mL). The filtrate was recovered and evaporated. The solid product was dried in vacuo, affording 3-(bromomethyl)-2, 4-dichloropyridine (2.9 g , 99% yield). The product was used without further purification.
Used for preparation of imidazo[4,5-b]pyridine derivatives for treatment of diseases caused by gastric acid.
Computed Properties
Molecular Weight:162.01
XLogP3:2.8
Hydrogen Bond Acceptor Count:1
Exact Mass:160.9799046
Monoisotopic Mass:160.9799046
Topological Polar Surface Area:12.9
Heavy Atom Count:9
Complexity:97.1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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