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Chemical Structure| 1040264-49-0 Chemical Structure| 1040264-49-0

Structure of 1040264-49-0

Chemical Structure| 1040264-49-0

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Product Details of [ 1040264-49-0 ]

CAS No. :1040264-49-0
Formula : C17H26N2O5
M.W : 338.40
SMILES Code : O=C(C1C(N)=CC(OC)=C(OCCCN2CCOCC2)C=1)OCC

Safety of [ 1040264-49-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1040264-49-0 ]

* 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 [ 1040264-49-0 ]

[ 1040264-49-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1040264-49-0 ]
  • [ 3473-63-0 ]
  • [ 199327-61-2 ]
YieldReaction ConditionsOperation in experiment
In methanol; for 6h;Reflux; Example 10: Preparation of 7-methoxy-6-(3-morpholin-4-ylpropoxy)-3/f-quinazolin-4-one; 4-Methoxy-5-(3-mophiholin-4-ylpropoxy)-2-nitrobenzoic acid ethyl ester (50g) was hydrogenated using 10percent palladium on carbon (50percent wet, 5g) in methanol (250ml) at" 3.0-3.5 kg/cm2 for 3 hours. After completion of reaction, catalyst was removed by filtration. Formamidine acetate (22g) in methanol was added to resulting filtrate and refluxed for 6 hours. After completion of reaction, the reaction mass was cooled to room temperature, stirred for 2 hours. The resulting product was filtered, washed with methanol (50 ml) and dried to betaive 33g (73percent) of the title compound.
 

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