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Chemical Structure| 77168-84-4 Chemical Structure| 77168-84-4

Structure of 77168-84-4

Chemical Structure| 77168-84-4

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Product Details of [ 77168-84-4 ]

CAS No. :77168-84-4
Formula : C7H8N2O3
M.W : 168.15
SMILES Code : O=C(C(N=C1C)=CNC1=O)OC
MDL No. :MFCD15144473

Safety of [ 77168-84-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 77168-84-4 ]

* 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 [ 77168-84-4 ]

[ 77168-84-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 77168-84-4 ]
  • [ 77168-85-5 ]
YieldReaction ConditionsOperation in experiment
52% With trichlorophosphate; In N,N-dimethyl-formamide; Example 47 METHYL 5-CHLORO-6-METHYL-2-PYRAZINE CARBOXYLATE To a solution of methyl 4,5-dihydro-6-methyl-5-oxo-2-pyrazine carboxylate (M. Mano, T. Seo, K. Imai, Chem. Pharm. Bull 10:3057-3063, 1980) in DMF (20 mL) was added POCl3 (20 mL). The reaction was refluxed for 0.5 h and then poured into ice. The aqueous layer was extracted with CHCl3 dried (MgSO4) and concentrated. The residue was chromatographed (SiO2, CHCl3) to provide the title compound (2.34 g, 52% yield); m.p. 49-50 C.
With N,N-dimethyl-formamide; trichlorophosphate; at 5 - 110℃; for 3.0h; Step 4, methyl 5-chloro-6-methylpyrazine-2-carboxylate To a stirred solution of methyl 6- methyl-5-oxo-4,5-dihydropyrazine-2-carboxylate (75 g, 0.446 mol) in phosphorous oxychloride (375 mL) was added DMF (5 mL) at 5-10 C. The reaction mixture was heated to 110 C for 3 h. Then the POCf was distilled off from the reaction mixture. The resulting residue was quenched with ice-cold water (300 mL) and extracted with dichloromethane (3 x 500 mL). The combined organic layers were washed with water (500 mL), brine (300 mL), dried over anhydrous sodium sulfate and concentrated to afford a crude residue. The crude residue was adsorbed on 150 g of 100-200 silica gel, which was then loaded over a pre-packed column with silica gel and gradient eluted with 12 % ethyl acetate/petroleum ether to 18 % ethyl acetate/petroleum ether to give the title compound
 

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