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1005515-30-9

4-chloro-6-methylnicotinoyl chloride synthesis

3synthesis methods
33821-58-8 Synthesis
CHEMBRDG-BB 4002882

33821-58-8
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$46.00/1g

4-chloro-6-methylnicotinoyl chloride

1005515-30-9
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Yield:1005515-30-9 94.2%

Reaction Conditions:

with trichlorophosphate at 95; for 16 h;

Steps:

A Step A:

6-Methyl-4-oxo-l,4-dihydropyridine-3 -carboxylic acid (50.0 g, 326.51 mmol) was suspended in phosphoryl trichloride (500.0 g, 3.26 mol) and stirred at 95°C for 16 h. After cooling, the excess phosphorus oxychloride was distilled off in vacuo, and obtained residue was evaporated with toluene (2x250 mL) to give 5-(carboxy)-4-chloro-2-methylpyridin-l- ium chloride (73.3 g, 95.0% purity, 307.46 mmol, 94.2% yield) .

References:

WO2020/221826,2020,A1 Location in patent:Page/Page column 114-115

67367-33-3 Synthesis
4-Hydroxy-6-methylnicotinic acid

67367-33-3
203 suppliers
$6.00/5g

4-chloro-6-methylnicotinoyl chloride

1005515-30-9
2 suppliers
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