4-Chloro-5-fluoro-2-methoxypyrimidine

4-Chloro-5-fluoro-2-methoxypyrimidine Suppliers list
Company Name: PharmaBlock Sciences (Nanjing),Inc.  
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Email: sales@pharmablock.com
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Company Name: UHN Shanghai Research & Development Co., Ltd.  
Tel: 021-58958002 18930822973
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Company Name: Guangzhou Isun Pharmaceutical Co., Ltd  
Tel: 020-39119399 18927568969
Email: isunpharm@qq.com

4-Chloro-5-fluoro-2-methoxypyrimidine manufacturers

4-Chloro-5-fluoro-2-methoxypyrimidine Basic information
Product Name:4-Chloro-5-fluoro-2-methoxypyrimidine
Synonyms: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%;4-Chloro-5-fluoro-2-methoxypyrimidine
CAS:1801-06-5
MF:C5H4ClFN2O
MW:162.55
EINECS:
Product Categories:
Mol File:1801-06-5.mol
4-Chloro-5-fluoro-2-methoxypyrimidine Structure
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
Safety Information
HS Code 2933599590
MSDS Information
4-Chloro-5-fluoro-2-methoxypyrimidine Usage And Synthesis
Synthesis
2-Methoxy-5-fluorouracil

1480-96-2

4-CHLORO-5-FLUORO-2-METHOXYPYRIMIDINE

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
4-Chloro-5-fluoro-2-methoxypyrimidine Preparation Products And Raw materials
Raw materials2-Methoxy-5-fluorouracil-->Toluene-->trichlorophosphate-->Triethylamine
Preparation Products2-Methoxy-5-fluoro-4-aminopyrimidine
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