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ChemicalBook--->CAS DataBase List--->43212-41-5

43212-41-5

43212-41-5 Structure

43212-41-5 Structure
IdentificationBack Directory
[Name]

2,4-Dichloro-6-methoxypyrimidine
[CAS]

43212-41-5
[Synonyms]

2,4-Dichloro-6-methoxypyrimidine
2,6-Dichloro-4-methoxypyrimidine
2,4-Dichloro-6-methoxy-1,3-diazine
Pyrimidine, 2,4-dichloro-6-methoxy-
2,4-Dichloro-6-methoxypyrimidine,>97%
2,4-Dichloro-6-methoxypyrimidine ISO 9001:2015 REACH
[Molecular Formula]

C5H4Cl2N2O
[MDL Number]

MFCD00955635
[MOL File]

43212-41-5.mol
[Molecular Weight]

179
Chemical PropertiesBack Directory
[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)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C5H4Cl2N2O/c1-10-4-2-3(6)8-5(7)9-4/h2H,1H3
[InChIKey]

ZSNZDRHTTWBNGI-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC(OC)=CC(Cl)=N1
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Warning
[Hazard statements ]

H317-H351b
[Precautionary statements ]

P201-P202-P261-P272-P280g-P302+P352-P308+P313-P363-P403-P501c
[Hazard Codes ]

Xn
[Risk Statements ]

22-36
[Safety Statements ]

26
[HS Code ]

2933599590
Hazard InformationBack Directory
[Uses]

2,4-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
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-Dichloro-6-methoxypyrimidine(43212-41-5)1HNMR
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