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Chemical Structure| 1480-96-2 Chemical Structure| 1480-96-2
Chemical Structure| 1480-96-2

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Synonyms: 5-Fluoro-4-hydroxy-2-methoxypyrimidine

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Product Details of 5-Fluoro-2-methoxypyrimidin-4(3H)-one

CAS No. :1480-96-2
Formula : C5H5FN2O2
M.W : 144.10
SMILES Code : O=C1NC(OC)=NC=C1F
Synonyms :
5-Fluoro-4-hydroxy-2-methoxypyrimidine
MDL No. :MFCD03265437
InChI Key :VMIFBCPINLZNNI-UHFFFAOYSA-N
Pubchem ID :352550

Safety of 5-Fluoro-2-methoxypyrimidin-4(3H)-one

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 5-Fluoro-2-methoxypyrimidin-4(3H)-one

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1480-96-2 ]

[ 1480-96-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1480-96-2 ]
  • [ 1801-06-5 ]
YieldReaction ConditionsOperation in experiment
95% With triethylamine; trichlorophosphate; In toluene; at 50 - 80℃; The 14.4g type IV compounds add 29 ml of toluene and 15.2g in triethylamine, heating to 50-80°C, dropwise 18.4g phosphorus oxychloride, the drop finishes, preserving heat and stirring reaction 5-7 hours, cooling to room temperature, adding water, separating, collecting the organic phase, organic phase is concentrated under reduced pressure, compound III namely type (strawcoloured liquid) 15.4g, molar yield is 95.0percent, HPLC purity of 95.8percent.
34% With N,N-dimethyl-aniline; trichlorophosphate; at 110℃; for 1.5h; 43b2-Methoxy-5-fluorouracil (43a, 1.04g, 7.21 mmol) and N,N-dimethylaniline (1.80 mL) were heated in POCI3 at 11O0C for 90 minutes. After cooling, the reaction was added carefully to ice. The product was extracted with diethylether. The ether layer was washed with sequentially with 2N HCI, water, and brine followed by drying (MgSO4). The ether was carefully removed under reduced pressure to give 43b as a volatile liquid (0.39g, 34percent) which was used without further purification. Rf = 0.26 (10percent EtOAc/hexane). 1H NMR (400MHz, DMSO-d6): delta 3.91 (s, 3H), 8.79 (s, 1 H)
 

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