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Chemical Structure| 1346462-59-6 Chemical Structure| 1346462-59-6

Structure of 1346462-59-6

Chemical Structure| 1346462-59-6

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Product Details of [ 1346462-59-6 ]

CAS No. :1346462-59-6
Formula : C7H11N3
M.W : 137.18
SMILES Code : NC1=CC(C)=NN1C2CC2
MDL No. :MFCD26518913

Safety of [ 1346462-59-6 ]

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 [ 1346462-59-6 ]

* 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 [ 1346462-59-6 ]

[ 1346462-59-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1346462-59-6 ]
  • [ 21080-80-8 ]
  • [ 1427853-84-6 ]
YieldReaction ConditionsOperation in experiment
310 mg With acetic acid; for 2h;Reflux; d ) Ethyl 1 ,6-dicyclopr opyl-3-methyl- lH-pyrazolo [3,4-6] pyridine-4-carboxylatel-cyclopropyl-3 -methyl- lH-pyrazol-5 -amine (300 mg, 2.187 mmol), ethyl 4-cyclopropyl- 2,4-dioxobutanoate (403 mg, 2.187 mmol) and acetic Acid (40 mL) were heated at reflux for 2 hours. The solvent was removed in vacuo and the crude residue was purified via silica gel chromatography (eluent: 0 to 11percent EtOAc:Hex). The product was collected as310mg. 1H NMR (400 MHz, CHLOROFORM-d) delta ppm 1.05 - 1.13 (m, 4 H), 1.16 - 1.21 (m, 2 H), 1.25 - 1.30 (m, 2 H), 1.46 (t, J=7.20 Hz, 3 H), 2.16 - 2.31 (m, 1 H), 2.63 (s, 3 H), 3.78 (m, J=7.26, 7.26, 3.79, 3.66 Hz, 1 H), 4.47 (q, J=7.24 Hz, 2 H), 7.40 (s, 1 LCMS(ES) [M+H]+ 286.2
 

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