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Chemical Structure| 16744-98-2 Chemical Structure| 16744-98-2

Structure of 16744-98-2

Chemical Structure| 16744-98-2

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Product Details of [ 16744-98-2 ]

CAS No. :16744-98-2
Formula : C7H4FNO
M.W : 137.11
SMILES Code : FC1=CC=CC=C1N=C=O
MDL No. :MFCD00001996
InChI Key :VZNCSZQPNIEEMN-UHFFFAOYSA-N
Pubchem ID :85588

Safety of [ 16744-98-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H301-H311-H315-H319-H331-H334-H335
Precautionary Statements:P210-P240-P241-P242-P243-P261-P264-P270-P271-P280-P285-P301+P310-P303+P361+P353-P304+P340-P305+P351+P338-P311-P330-P363-P370+P378-P403+P233-P405-P501
Class:6.1(3)
UN#:3080
Packing Group:

Application In Synthesis of [ 16744-98-2 ]

* 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 [ 16744-98-2 ]

[ 16744-98-2 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 123-75-1 ]
  • [ 16744-98-2 ]
  • [ 774-07-2 ]
  • 3-(2-fluorophenyl)-7-pyrrolidin-1-yl-1H-pyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione [ No CAS ]
  • 2
  • [ 123-75-1 ]
  • [ 16744-98-2 ]
  • [ 17201-43-3 ]
  • [ 774-07-2 ]
  • 4-[3-(2-fluorophenyl)-2,4-dioxo-7-pyrrolidin-1-yl-3,4-dihydro-2H-pyrimido[4,5-d]pyrimidin-2-ylmethyl]benzonitrile [ No CAS ]
  • 3
  • [ 123-75-1 ]
  • [ 16744-98-2 ]
  • [ 774-07-2 ]
  • [ 5332-06-9 ]
  • 4-[3-(2-fluoro-phenyl)-2,4-dioxo-7-pyrrolidin-1-yl-3,4-dihydro-2<i>H</i>-pyrimido[4,5-<i>d</i>]pyrimidin-1-yl]-butyronitrile [ No CAS ]
  • 4
  • [ 123-00-2 ]
  • [ 16744-98-2 ]
  • [ 7051-34-5 ]
  • [ 774-07-2 ]
  • 1-cyclopropylmethyl-3-(2-fluoro-phenyl)-7-(3-morpholin-4-yl-propylamino)-1<i>H</i>-pyrimido[4,5-<i>d</i>]pyrimidine-2,4-dione [ No CAS ]
  • 5
  • [ 16744-98-2 ]
  • [ 63746-12-3 ]
  • C16H11FN2O4 [ No CAS ]
  • 6
  • [ 16744-98-2 ]
  • [ 110223-15-9 ]
  • 1-(3-(benzyloxy)pyrazin-2-yl)-3-(2-fluorophenyl)urea [ No CAS ]
YieldReaction ConditionsOperation in experiment
69.43% In tetrahydrofuran; for 8h;Reflux; <strong>[110223-15-9]3-(benzyloxy)pyrazin-2-amine</strong> (100 mg, 0.5 mmol) and 2-fluoro isocyanate (0.67 mL, 0.60 mmol) in tetrahydrofuran (0.25 M) was dissolved in 8 hours during the heating under reflux thereby. After completion of the reaction, and concentrating the solvent under reduced pressure. The residue was washed with methanol and vacuum filter to give 122.6 mg of the desired compound in a yield of 69.43%.
69.4% In tetrahydrofuran;Inert atmosphere; Schlenk technique; Reflux; General procedure: 2-Amino-3-benzyloxypyridine or pyrazine derivative(2.5 mmol) was dissolved in dry THF (10 mL), isocyanate derivative(3.0 mmol) was added to the reaction mixture. The reaction wasrefluxed for 3-6 h. After cooling, the reaction mixture was evaporated and the residue was purified by solidification with cold methanol and filtered to give the target compounds.
 

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