4-Chloro-6-methoxypyrimidine
4-Chloro-6-methoxypyrimidine Basic information
- Product Name:
- 4-Chloro-6-methoxypyrimidine
- Synonyms:
-
- 6-CHLORO-4-PYRIMIDINYL METHYL ETHER
- 4-CHLORO-6-METHOXYPYRIMIDINE
- Pyrimidine, 4-chloro-6-methoxy- (6CI,8CI,9CI)
- 4-Chloro-6-methoxy-1,3-diazine
- 4-chloro-6-methoxypyrimidine(SALTDATA: FREE)
- 4-Chloro-6-methoxypyrimidine 98+%
- Pyrimidine, 4-chloro-6-methoxy-
- 4-Chloro-6-MethoxypyriMidine, 98.0%(GC)
- CAS:
- 26452-81-3
- MF:
- C5H5ClN2O
- MW:
- 144.56
- EINECS:
- 678-369-8
- Product Categories:
-
- Heterocycle-Pyrimidine series
- alkyl chloride
- PYRIMIDINE
- APIs & Intermediate
- API intermediates
- Mol File:
- 26452-81-3.mol
4-Chloro-6-methoxypyrimidine Chemical Properties
- Melting point:
- 34.5-35.0 °C
- Boiling point:
- 80°C/18mmHg(lit.)
- Density
- 1.292±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- powder to lump to clear liquid
- pka
- -1.59±0.17(Predicted)
- color
- White or Colorless to Light yellow
- InChI
- InChI=1S/C5H5ClN2O/c1-9-5-2-4(6)7-3-8-5/h2-3H,1H3
- InChIKey
- KLJGSQVYUGQOAW-UHFFFAOYSA-N
- SMILES
- C1=NC(OC)=CC(Cl)=N1
- CAS DataBase Reference
- 26452-81-3(CAS DataBase Reference)
4-Chloro-6-methoxypyrimidine Usage And Synthesis
Uses
4-Chloro-6-methoxypyrimidine could be the starting material for preparing 4-chloro-6-hydroxypyrimidine.
Synthesis
67-56-1
1193-21-1
26452-81-3
A) Methanol (5.4 mL) was slowly added dropwise to a suspension of tetrahydrofuran (THF, 200 mL) containing 60% sodium hydride (8.05 g) under nitrogen protection, keeping the reaction temperature at 0 °C. Subsequently, a solution of 4,6-dichloropyrimidine (20.0 g) in THF (45 mL) was added to the reaction system at 0 °C, and the reaction continued to be stirred at 0 °C for 1 hour. Upon completion of the reaction, 1N hydrochloric acid was slowly added to the reaction mixture at 0 °C for neutralization, followed by extraction of the reaction product with ethyl acetate. The organic phase was washed sequentially with water and saturated brine and dried with anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure and the residue was recrystallized by hexane to afford the target product 4-chloro-6-methoxypyrimidine (10.2 g) as light yellow crystals. The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 3.96 (3H, s), 7.19 (1H, s), 8.69 (1H, s).
References
[1] Tetrahedron Letters, 2005, vol. 46, # 23, p. 3977 - 3979
[2] European Journal of Medicinal Chemistry, 2005, vol. 40, # 9, p. 862 - 874
[3] Patent: US2013/143870, 2013, A1. Location in patent: Paragraph 0267; 0268; 0269
[4] Patent: US2013/137688, 2013, A1. Location in patent: Paragraph 0221; 0222; 0223; 0224
[5] Patent: US2013/158038, 2013, A1. Location in patent: Paragraph 0134; 0135
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4-Chloro-6-methoxypyrimidine(26452-81-3)Related Product Information
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- 4-CHLORO-6-METHOXYQUINOLINE
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- 4-BENZYLOXY-6-CHLOROPYRIMIDINE
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