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[ CAS No. 182880-24-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 182880-24-6
Chemical Structure| 182880-24-6
Structure of 182880-24-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 182880-24-6 ]

CAS No. :182880-24-6 MDL No. :MFCD09998268
Formula : C9H8N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 176.17 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 182880-24-6 ]

* 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 [ 182880-24-6 ]

[ 182880-24-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 16064-10-1 ]
  • trichlorophosphate [ No CAS ]
  • [ 182880-24-6 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate; sodium In methanol 52.Y Y Y 6-Hydroxy-4-methoxyquinazoline A mixture of 200 mg of 6-hydroxy-3H-quinazolin-4-one and 5 ml of phosphorylchloride is heated to reflux for 2 hours. The excess phosphorylchloride is distilled off in vacuo and the residue is taken up in a solution of sodium methoxide (prepared from 80 mg sodium) in dry methanol. After refluxing for 2 hours the solvent is distilled off and the residue is partitioned between aqueous ph7-buffer solution and ethyl acetate. The organic phase is separated, dried over magnesium sulfate and evaporated in vacuo. The crude product is directly used in the next reaction or purified by chromatography on silica gel. 1 H-NMR (d6 -DMSO): 10.25 (br.s, 1H); 8.61 (s, 1H); 7.79 (d, J=9 Hz, 1H); 7.45 (dd,J=2.8+9 Hz, 1H); 7.32 (d,J=2.8 Hz, 1H); 4.09 (s,3H).
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