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Chemical Structure| 21427-85-0 Chemical Structure| 21427-85-0

Structure of 21427-85-0

Chemical Structure| 21427-85-0

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Product Details of [ 21427-85-0 ]

CAS No. :21427-85-0
Formula : C7H8N2O3
M.W : 168.15
SMILES Code : O=C(C(C=NN1)=CC1=O)OCC
MDL No. :MFCD18836660

Safety of [ 21427-85-0 ]

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 [ 21427-85-0 ]

* 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 [ 21427-85-0 ]

[ 21427-85-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 21427-85-0 ]
  • [ 867130-58-3 ]
  • 2
  • [ 867130-58-3 ]
  • [ 64-17-5 ]
  • [ 21427-85-0 ]
YieldReaction ConditionsOperation in experiment
83% Step 14C: Ethyl 6-oxo-1H-pyridazine-4-carboxylate; The compound of Step 14B was dissolved in EtOH (10 mL) and concentrated H2SO4 (4.2 mL) was added and then heated at reflux for 5 h. The reaction mixture was cooled, concentrated in vacuo and basified with saturated Na2CO2. After filtration, the aqueous phase was extracted with EtOAc, dried over anhydrous Na2SO4, filtered and concentrated to give the subtitle product (83%).1H NMR (400 MHz, CD3OD): delta 8.27 (d, 1H), 7.42 (d, 1H), 4.40 (q, 2H), 1.39 (t, 3H).
83% Step 10C: Ethyl 6-oxo-1,6-dihydropyridazine-4-carboxylate; The subtitle compound of step 10B was dissolved in EtOH (10 mL) and concentrated H2SO4 (4.2 mL) was added and then heated at reflux for 5 hours. The reaction mixture was cooled, concentrated in vacuo and basified with saturated Na2CO3. After filtration, the aqueous phase was extracted with ethyl acetate, dried over anhydrous Na2SO4, filtered and concentrated to give the subtitle compound (83%).1H NMR (400 MHz, MeOH-d4): delta 8.27 (d, 1H), 7.42 (d, 1H), 4.40 (q, 2H), 1.39 (t, 3H).
83% Step 7C: Ethyl 6-oxo-1,6-dihydropyridazine-4-carboxylate The subtitle product of Step 7B was dissolved in EtOH (10 mL) and concentrated H2SO4 (4.2 mL) was added and then heated at reflux for 5 hours. The reaction mixture was cooled, concentrated in vacuo and basified with saturated Na2CO3. After filtration, the aqueous phase was extracted with EtOAc, dried over anhydrous Na2SO4, filtered and concentrated to give the subtitle compound (83%).1H NMR (400 MHz, CD3OD): delta 8.27 (d, 1H), 7.42 (d, 1H), 4.40 (q, 2H), 1.39 (t, 3H).
83% With sulfuric acid; for 5.0h;Heating / reflux; Step 13C: Ethyl 6-oxo-1,6-dihydropyridazine-4-carboxylate The compound of step 13B was dissolved in EtOH (10 mL) and concentrated H2SO4 (4.2 mL) was added and then heated at reflux for 5 hours. The reaction mixture was cooled, concentrated in vacuo and basified with saturated Na2CO3. After filtration, the aqueous phase was extracted with ethyl acetate, dried over anhydrous Na2SO4, filtered and concentrated to give the subtitle compound (83%). 1H NMR (400 MHz, CD3OD): delta 8.27 (d, 1H), 7.42 (d, 1H), 4.40 (q, 2H), 1.39 (t, 3H).
With acetyl chloride; at 75℃; Example 39.1<strong>[867130-58-3]6-Oxo-1,6-dihydro-pyridazine-4-carboxylic acid</strong> ethyl ester The title compound from Example 38 (1.0 g, 7.13 mmol) was added to a solution of ethanol (16 mL) and acetyl chloride (4 mL) and the resulting suspension was heated to 75 C. and stirred overnight. The reaction mixture was concentrated, diluted with water and extracted with dichloromethane. The organic phase was dried over sodium sulfate, filtered and concentrated to give the title compound.1H NMR (300 MHz, CDCl3): delta (ppm) 10.91 (broad s, 1H), 8.26 (s, 1H), 7.53 (s, 1H), 4.43 (q, 2H), 1.40 (t, 3H).
With acetyl chloride; at 75℃; 6-Oxo-l,6-dihydro-pyridazine-4-carboxylic acid ethyl esterThe title compound from Example 18.3 (1.0 g, 7.13 mmol) was added to a solution of ethanol (16 mL) and acetyl chloride (4 mL) and the resulting suspension was heated to 75 C and stirred overnight. The reaction mixture was concentrated, diluted with water and extracted with dichloromethane. The organic phase was dried over sodium sulfate, filtered and concentrated to give the title compound.1H NMR (300 MHz, CDCl3) delta 10.91 (br, IH), 8.26 (s, IH), 7.53 (s, IH), 4.43 (q, 2H), 1.40 (t, 3H).

 

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