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2,4-Dichloro-6-methoxypyrimidine

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CAS:43212-41-5
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CAS:43212-41-5
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CAS:43212-41-5
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2,4-Dichloro-6-methoxypyrimidine manufacturers

2,4-Dichloro-6-methoxypyrimidine Basic information
Product Name:2,4-Dichloro-6-methoxypyrimidine
Synonyms:2,4-Dichloro-6-methoxypyrimidine;Pyrimidine, 2,4-dichloro-6-methoxy-;2,4-Dichloro-6-methoxy-1,3-diazine;2,6-Dichloro-4-methoxypyrimidine;2,4-Dichloro-6-methoxypyrimidine,>97%;2,4-Dichloro-6-methoxypyrimidine ISO 9001:2015 REACH
CAS:43212-41-5
MF:C5H4Cl2N2O
MW:179
EINECS:
Product Categories:Heterocycle-Pyrimidine series
Mol File:43212-41-5.mol
2,4-Dichloro-6-methoxypyrimidine Structure
2,4-Dichloro-6-methoxypyrimidine Chemical Properties
Boiling point 263.2±20.0 °C(Predicted)
density 1.446±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-4.54±0.30(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C5H4Cl2N2O/c1-10-4-2-3(6)8-5(7)9-4/h2H,1H3
InChIKeyZSNZDRHTTWBNGI-UHFFFAOYSA-N
SMILESC1(Cl)=NC(OC)=CC(Cl)=N1
Safety Information
Hazard Codes Xn
Risk Statements 22-36
Safety Statements 26
HS Code 2933599590
MSDS Information
2,4-Dichloro-6-methoxypyrimidine Usage And Synthesis
Uses2,4-Dichloro-6-methoxypyrimidine is an intermediate used to prepare piperazinyl pyrimidine derivatives as γ-secretase modulators. It is also used in the synthesis of α-azinylalkylamino-substituted (thiazolylamino)pyrimidines and -pyrazines as selective JAK2 inhibitors.
Synthesis
6-METHOXYURACIL

29458-38-6

2,4-Dichloro-6-methoxypyrimidine

43212-41-5

General procedure for the synthesis of 2,4-dichloro-6-methoxypyrimidine from 6-methoxypyrimidine-2,4(1H,3H)-dione: 6-methoxypyrimidine-2,4(1H,3H)-dione (15 g, 0.106 mol) was mixed with phosphorus triclosan (400 ml) and heated and refluxed for 4 h. After completion of the reaction the excess of phosphorus triclosan was removed by distillation under reduced pressure. The residue was quenched with an ice-water mixture and extracted with ethyl acetate (EtOAc). The organic phases were combined, washed with water, dried over anhydrous sodium sulfate (Na2SO4), and concentrated under reduced pressure to remove the solvent to afford 2,4-dichloro-6-methoxypyrimidine as an oil (5.5 g, 30% yield). Nuclear Magnetic Resonance Hydrogen Spectroscopy (NMR) data: δ 3.96 (3H, single peak), 6.63 (1H, single peak); Mass Spectrum (m/z): 179 [MH]+.

References[1] Patent: WO2007/31745, 2007, A1. Location in patent: Page/Page column 96
[2] Organic Process Research and Development, 2012, vol. 16, # 8, p. 1416 - 1421
[3] Patent: WO2006/109026, 2006, A1. Location in patent: Page/Page column 97
[4] Patent: WO2008/117051, 2008, A1. Location in patent: Page/Page column 29
[5] Patent: WO2016/168619, 2016, A1. Location in patent: Paragraph 00162
2,4-Dichloro-6-methoxypyrimidine Preparation Products And Raw materials
Raw materials6-METHOXYURACIL-->2,4,6-Trichloropyrimidine-->Sodium Methoxide
Tag:2,4-Dichloro-6-methoxypyrimidine(43212-41-5) Related Product Information
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