4-CHLORO-5-FLUORO-2-METHOXYPYRIMIDINE
4-CHLORO-5-FLUORO-2-METHOXYPYRIMIDINE Basic information
- Product Name:
- 4-CHLORO-5-FLUORO-2-METHOXYPYRIMIDINE
- Synonyms:
-
- 4-CHLORO-5-FLUORO-2-METHOXYPYRIMIDINE
- PyriMidine, 4-chloro-5-fluoro-2-Methoxy-
- 2-Methoxy-4-chloro-5-fluoropyrimidine
- 4-Chloro-5-fluoro-2-methoxypyrimidine (Capecitabine Impurity)
- Capecitabine Impurity 35
- 2-Chloro-5-fluoro-2-methoxypyrimidine 95%
- CAS:
- 1801-06-5
- MF:
- C5H4ClFN2O
- MW:
- 162.55
- Mol File:
- 1801-06-5.mol
4-CHLORO-5-FLUORO-2-METHOXYPYRIMIDINE Chemical Properties
- Boiling point:
- 86-87 °C(Press: 21 Torr)
- Density
- 1.400±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- solubility
- DMSO
- pka
- -1.34±0.29(Predicted)
- form
- Oil
- color
- Colourless
- Stability:
- Moisture Sensitive
4-CHLORO-5-FLUORO-2-METHOXYPYRIMIDINE Usage And Synthesis
Synthesis
1480-96-2
1801-06-5
General procedure for the synthesis of 2-methoxy-4-chloro-5-fluoropyrimidine from 2-methoxy-5-fluorouracil: 14.4 g of 2-methoxy-5-fluorouracil (compound IV) was dissolved in 29 mL of toluene and 15.2 g of triethylamine was added as a base. The reaction mixture was heated to 50-80 °C and 18.4 g of trichlorophosphorus was slowly added dropwise. After the dropwise addition, the temperature was maintained and the reaction was continued with stirring for 5-7 hours. After completion of the reaction, the mixture was cooled to room temperature and quenched by addition of water. The organic and aqueous phases were separated and the organic phase was collected. The organic phase was concentrated under reduced pressure to remove the solvent to afford 15.4 g of 2-methoxy-4-chloro-5-fluoropyrimidine (Compound III, straw-colored liquid) in 95.0% molar yield and 95.8% HPLC purity.
References
[1] Patent: CN105272922, 2016, A. Location in patent: Paragraph 0035; 0036; 0037
[2] Patent: WO2006/72831, 2006, A1. Location in patent: Page/Page column 66
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