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Chemical Structure| 672-81-1 Chemical Structure| 672-81-1

Structure of 672-81-1

Chemical Structure| 672-81-1

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Product Details of [ 672-81-1 ]

CAS No. :672-81-1
Formula : C5H4N2O
M.W : 108.10
SMILES Code : N#CC(C#N)=COC
MDL No. :MFCD07437817

Safety of [ 672-81-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H317-H334
Precautionary Statements:P261-P264-P270-P272-P280-P285-P302+P352-P304+P341-P310-P330-P333+P313-P363-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 672-81-1 ]

* 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 [ 672-81-1 ]

[ 672-81-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 672-81-1 ]
  • [ 6971-45-5 ]
  • [ 650628-19-6 ]
YieldReaction ConditionsOperation in experiment
53% With sodium methylate; In ethanol; for 18h;Heating / reflux; To a solution of 1-(2-methoxyphenyl)hydrazine hydrogen chloride (3 g, 0.017 mol) in ethanol (50 mL) was added 2-(methoxymethylene)malononitrile (1.89 g, 0.9 eq.) and sodium methoxide (1.92 g, 2.1 eq). The reaction mixture was heated at reflux for 18 h and concentrated. The reaction mixture was partitioned between brine and ethyl acetate. The organic layer was separated, dried with magnesium sulfate, filtered and concentrated. MPLC Biotage chromatography eluding with 20-60% ethyl acetate/hexanes afforded the title compound in 53% yield (1.9 g). 400 MHz 1H NMR (CDCl3) delta 7.64 (m, 1 H), 7.40 (m, 2H), 7.08 (m,2H), 4.51 (bs, 2H), 3.87 (s, 3 H); MS: (M+H m/z=215.2).
53% With sodium methylate; In ethanol; for 18h;Heating / reflux; a) 5-amiotano-1 -(2-methoxyphenyl)-1 H-pyrazole-4-carboniotatriotaleTo a solution of 1 -(2-methoxyphenyl)hydraziotane hydrogen chloride (3g, O 017 mol) in ethanol (50 mL) was added 2-(methoxymethylene)malononiotatriotale (1 89 g, 0 9 eq ) and sodium methoxide (1 92g, 2 1 eq) The reaction mixture was heated at reflux for 18h and concentrated The reaction mixture was partitioned between brine and ethyl acetate The organic layer was separated, dried with magnesium sulfate, filtered and concentrated MPLC Biotage chromatography eluting with 20-60% ethyl acetate/hexanes afforded the title compound in 53% yield (1 9g) 400 MHz 1 H NMR (CDCI3) delta 7 64 (m, <n="50"/>1 H), 7 40 (m, 2H), 7 08 (m,2H), 4 51 (bs 2H), 3 87 (s, 3 H), MS (M+H m/z =215
  • 2
  • [ 672-81-1 ]
  • [ 823-85-8 ]
  • [ 51516-70-2 ]
YieldReaction ConditionsOperation in experiment
60% With triethylamine; In ethanol; for 16h;Reflux; 2-(Methoxymethylene)malononitrile (1.00 g, 8.19 mmol), (4-fluorophenyl) hydrazine hydrochloride (1.40 g, 8.61 mmol), triethylamine (1.66 g, 16.4 mmol) and ethanol (50 mE) were added to a 100-mE round-bottom flask fitted with a magnetic stir bar and condenser. The resulting solution was heated at reflux for 16 h. The resulting mixture was concentrated under vacuum. The residue was purified by colunm chromatography eluting with dichloromethane/ methanol (10:1 v/v)to give 5-amino-i-(4-fluorophenyl)-1H- pyrazole-4-carbonitrile (1.00 g, 60%). ECMS: (ESI) mlz 203 [M+H].
  • 3
  • [ 672-81-1 ]
  • [ 143-37-3 ]
  • [ 698-29-3 ]
YieldReaction ConditionsOperation in experiment
26% To a suspension of 50 (387 g, 40.9 mmoi) in EtOH (10 mL) is added a solution of sodium methoxide (2.2 g. 40.9 nunol) in F:tOH (10 rnL). After stirring at room temperature for 40 minutes, the mixture is filtered and the solid is washed with EtOH (1 mL). The filtrate is then treated with 49 (2.5 g, 20.5 mmol) and the resulting solid is collected by filtration and dried to give 51 (700 ing, 26%). (MS: [MH-Hj 109.0)
 

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