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Chemical Structure| 25412-66-2 Chemical Structure| 25412-66-2

Structure of 25412-66-2

Chemical Structure| 25412-66-2

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Product Details of [ 25412-66-2 ]

CAS No. :25412-66-2
Formula : C8H10N2O
M.W : 150.18
SMILES Code : N=C(N)C1=CC=CC(OC)=C1
MDL No. :MFCD05663319
InChI Key :ZSHGVAIVMZVMPD-UHFFFAOYSA-N
Pubchem ID :5108695

Safety of [ 25412-66-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 25412-66-2 ]

* 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 [ 25412-66-2 ]

[ 25412-66-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 25412-66-2 ]
  • [ 58483-95-7 ]
  • C14H10ClN3O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With sodium acetate; In 2-methoxy-ethanol; at 70℃; for 10h; General procedure: A mixture of compound <strong>[58483-95-7]5-amino-2-chloropyridine-4-carboxylic acid</strong>(1000 g, 5.8 mol) was dissolved in 5000 mlEthylene glycol monomethyl ether, AddedFormamidine hydrochloride(1867 g, 23.2 mol), sodium acetate (2360 g, 17.4 mol). The reaction was heated to 120 ° C for 6 hours. After the reaction was complete, the reaction was cooled to room temperature, poured into 4000 ml of water and extracted twice with ethyl acetate. The organic phase was combined, dried and concentrated to afford the crude product which was filtered to give 6-chloropyridine And [3,4-d] pyrimidin-4 (3H) ketone (924 g, 5-1 mol)
 

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