ChemicalBook--->CAS DataBase List--->1192479-35-8

1192479-35-8

1192479-35-8 Structure

1192479-35-8 Structure
IdentificationBack Directory
[Name]

2-CHLORO-5-FLUORO-4-METHOXY-6-METHYLPYRIMIDINE
[CAS]

1192479-35-8
[Synonyms]

2-CHLORO-5-FLUORO-4-METHOXY-6-METHYLPYRIMIDINE
Pyrimidine, 2-chloro-5-fluoro-4-methoxy-6-methyl-
[Molecular Formula]

C6H6ClFN2O
[MDL Number]

MFCD16621230
[MOL File]

1192479-35-8.mol
[Molecular Weight]

176.58
Chemical PropertiesBack Directory
[Boiling point ]

278.4±35.0 °C(Predicted)
[density ]

1.334±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-0.33±0.39(Predicted)
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

2-CHLORO-5-FLUORO-4-METHOXY-6-METHYLPYRIMIDINE(1192479-35-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,4-Dichloro-5-fluoro-6-methylpyrimidine

954220-98-5

Sodium Methoxide

124-41-4

2-CHLORO-5-FLUORO-4-METHOXY-6-METHYLPYRIMIDINE

1192479-35-8

To a solution of tetrahydrofuran (THF, 6 mL) containing 2,4-dichloro-5-fluoro-6-methylpyrimidine (563 mg, 3.11 mmol), a methanolic solution of 25% sodium methanolate (671 mg) was slowly added under cooling at 0°C. The reaction mixture was slowly warmed up to room temperature over 1 hour. After completion of the reaction, the reaction solution was diluted with water and extracted with ethyl acetate (EtOAc). The organic phases were combined, concentrated and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to afford 2-chloro-5-fluoro-4-methoxy-6-methylpyrimidine in quantitative yield.

[References]

[1] Patent: WO2009/131974, 2009, A1. Location in patent: Page/Page column 88
[2] Patent: WO2014/66132, 2014, A1. Location in patent: Page/Page column 16-17
[3] Patent: WO2012/138590, 2012, A1. Location in patent: Page/Page column 71-72
[4] Journal of Medicinal Chemistry, 2016, vol. 59, # 7, p. 3231 - 3248
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