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Chemical Structure| 374067-80-8 Chemical Structure| 374067-80-8

Structure of 374067-80-8

Chemical Structure| 374067-80-8

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Product Details of [ 374067-80-8 ]

CAS No. :374067-80-8
Formula : C11H8N4O2
M.W : 228.21
SMILES Code : N#CC1=CC=C(NC2=NC(O)=CC(N2)=O)C=C1
MDL No. :MFCD17015090

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Application In Synthesis of [ 374067-80-8 ]

* 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 [ 374067-80-8 ]

[ 374067-80-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5637-42-3 ]
  • [ 105-53-3 ]
  • [ 374067-80-8 ]
YieldReaction ConditionsOperation in experiment
With ethanol; sodium; for 12h;Reflux; Diethyl malonate (30 gm) was added to l-<strong>[5637-42-3](4-cyanophenyl)guanidine</strong> (30 gm) at room temperature. A solution of sodium (17.2 gm) in ethanol (450 ml) was added to the above reaction mass. The contents were heated to reflux and maintained for 12 hours. Distilled off the solvent completely under vacuum and then added water (500 ml). The reaction mass was stirred for 30 minutes and filtered. The solid obtained was dried to obtain 40 gm of 4-(4,6-dihydroxypyrimidine-2-yl-amino)benzonitrile.
40g With ethanol; sodium; for 12h;Reflux; Diethyl malonate (30 gm) was added to <strong>[5637-42-3]1-<strong>[5637-42-3](4-cyanophenyl)guanidine</strong></strong> (30 gm) at room temperature. A solution of sodium (17.2 gm) in ethanol (450 ml) was added to the above reaction mass. The contents were heated to reflux and maintained for 12 hours. Distilled off the solvent completely under vacuum and then added water (500 ml). The reaction mass was stirred for 30 minutes and filtered. The solid obtained was dried to obtain 40 gm of 4-(4,6-dihydroxypyrimidine-2-yl-amino)benzonitrile.
6.5 g With methanol; sodium; In methanol; for 6h;Reflux; Inert atmosphere; 5.7 g of sodium metal was added to 200 mL of methanol at 0-5 C. with constant stirring under nitrogen atmosphere. 10 g of compound II dissolved in 200 mL of methanol was added to the solution followed by the dropwise addition of 10 g of diethyl malonate. The reaction mixture was heated to reflux for 6 h. After completion of the reaction, the solvent was removed under vacuum; water was added to the crude mixture and stirred for 30 minutes. The solid was filtered and adjusted the pH of the filtrate to 4.0-6.0. The separated solid was filtered, washed with acetone and dried to give 6.5 g of a solid.
 

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