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4-METHYL-6-CHLORO PYRIMIDINE

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4-METHYL-6-CHLORO PYRIMIDINE manufacturers

4-METHYL-6-CHLORO PYRIMIDINE Basic information
Product Name:4-METHYL-6-CHLORO PYRIMIDINE
Synonyms:AKOS BBS-00002134;Pyrimidine, 4-chloro-6-methyl- (6CI,7CI,8CI,9CI);4-chloro-6-methylpyrimidine(SALTDATA: FREE);6-Chloro-4-methylpyrimidine;4-Chloro-6-methyl-1,3-diazine;Pyrimidine, 4-chloro-6-methyl-;4-Chloro-6-methylpyrimidine,97%;4-METHYL-6-CHLORO PYRIMIDINE ISO 9001:2015 REACH
CAS:3435-25-4
MF:C5H5ClN2
MW:128.56
EINECS:685-585-6
Product Categories:Heterocycle-Pyrimidine series;PYRIMIDINE;Halides;Pyrazines, Pyrimidines & Pyridazines
Mol File:3435-25-4.mol
4-METHYL-6-CHLORO PYRIMIDINE Structure
4-METHYL-6-CHLORO PYRIMIDINE Chemical Properties
Melting point 151-152℃
Boiling point 195℃
density 1.234
Fp 90℃
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form Solid
pka0.83±0.17(Predicted)
color Pale yellow
Water Solubility Slightly soluble in water.
Safety Information
HS Code 2933599590
MSDS Information
4-METHYL-6-CHLORO PYRIMIDINE Usage And Synthesis
UsesIt is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.
Synthesis
4,6-Dichloropyrimidine

1193-21-1

Methylmagnesium Bromide

75-16-1

4-METHYL-6-CHLORO PYRIMIDINE

3435-25-4

To a solution of 4,6-dichloropyrimidine (1.0 g, 6.71 mmol) in tetrahydrofuran (30 mL) was added sequentially 1-methyl-2-pyrrolidinone (3.2 mL, 6.71 mmol), iron(III) acetylacetonate (0.119 g, 0.336 mmol) and methylmagnesium bromide (2.237 mL, 6.71 mmol). The reaction mixture was stirred at room temperature for 3 h. After completion of the reaction, the reaction was quenched with water and extracted with ethyl acetate (100 mL). The organic layer was separated and concentrated under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (eluent: 20% ethyl acetate/hexane) to afford 4-chloro-6-methylpyrimidine (0.6 g, 3.08 mmol, 46% yield) as a colorless gelatinous liquid.LC-MS (ESI) analysis showed m/z 129.0 [M+H]+ (calculated value C5H6ClN2: 129.0); LC/MS retention time ( Method D): 1.36 min.

References[1] Patent: WO2017/59085, 2017, A1. Location in patent: Page/Page column 403; 404
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