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Chemical Structure| 1758-98-1 Chemical Structure| 1758-98-1

Structure of 1758-98-1

Chemical Structure| 1758-98-1

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Product Details of [ 1758-98-1 ]

CAS No. :1758-98-1
Formula : C5H6N2O3
M.W : 142.11
SMILES Code : COC1=NC(O)=CC(O)=N1
MDL No. :MFCD00209660
InChI Key :INZGPQPOYOLJOW-UHFFFAOYSA-N
Pubchem ID :13754312

Safety of [ 1758-98-1 ]

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

Application In Synthesis of [ 1758-98-1 ]

* 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 [ 1758-98-1 ]

[ 1758-98-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1758-98-1 ]
  • [ 1074-40-4 ]
YieldReaction ConditionsOperation in experiment
44% With trichlorophosphate; for 4.0h;Heating / reflux; Step 2; 4,6-dichloro-2-methoxy-pyrimidine; 2-Methoxy-pyrimidine-4,6-diol was dissolved in phosphorous oxychloride and the resultant reaction mixture was refluxed for four hours. After quenching with basic ice-water, the resultant aqueous mixture was extracted with ethyl acetate and the combined extracts dried <n="52"/>over magnesium sulfate. The organics were concentrated in vacuo yielding 1.1 g (44percent, crude yield) of the title compound.LCMS: Mass Found (M+l, 179)
14% Step 2: 4,6-dichloro-2-methoxypyrimidine; 2.25 g (7.92 mmol) 2-methoxypyrimidine-4,6-diol and 10.0 mL (108.92 mmol) phosphorus oxychloride were boiled for 2 h. The reaction mixture was poured onto alkaline ice water and made alkaline with NaOH. The aqueous phase was extracted with DCM. The organic phase was separated off, dried and evaporated down i.vac.Yield: 0.20 g (14percent of theory)ESI-MS: m/z=179 (M+H)+ Rt(HPLC): 1.38 min (method B)
 

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