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Chemical Structure| 1197943-43-3 Chemical Structure| 1197943-43-3

Structure of 1197943-43-3

Chemical Structure| 1197943-43-3

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Product Details of [ 1197943-43-3 ]

CAS No. :1197943-43-3
Formula : C9H12N2O2
M.W : 180.20
SMILES Code : O=CC=1C=NN(C1)C2OCCCC2
MDL No. :MFCD13188218

Safety of [ 1197943-43-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 1197943-43-3 ]

* 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 [ 1197943-43-3 ]

[ 1197943-43-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-87-2 ]
  • [ 35344-95-7 ]
  • [ 1197943-43-3 ]
YieldReaction ConditionsOperation in experiment
92% With trifluoroacetic acid; In tetrahydrofuran; at 90℃; for 4h; To a stirred solution of pyrazole carboxaldehyde (2-1, 300 mg, 3.1 mmol) in tetrahydrofuran was sequentially added 3,4-dihydro-2H-pyran (2-2, 867 mg, 10.3 mmol) and catalytic amount of trifluoroacetic acid. The resulting solution was refluxed for 4 h and then cooled to rt. The reaction was quenched by addition of trace amount of sodium hydride. Solvent was removed under vacuum and the residue was purified by silica gel chromatography to give 2-3 (520 mg, 92percent). MS (ESI+): m/z: 181.1 (M+H)+.
86% With toluene-4-sulfonic acid; In dichloromethane; at 20 - 60℃; for 10.5h; General procedure: para-Toluenesulfonic acid 206 mg (1.08 mmol) and DHP 1.85 ml (21.8 mmol) were added to a THF (30 ml)suspension of 1H-pyrazole-3-carbaldehyde 1.05 g (10.9 mmol), and the mixture was stirred at room temperature for 1hour. Next, methylene chloride 30 ml was added, and the mixture was stirred at room temperature for 4.5 hours and at60C for 5 hours. After the completion of the reaction, water was added to the reaction mixture, and followed by extractionwith ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and filtered. Thefiltrate was concentrated under reduced pressure. The concentrated residue was purified by silica gel column chromatography(eluting solvent: hexane: ethyl acetate) to give the title compound (including impurities).
 

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