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[ CAS No. 1383735-30-5 ] {[proInfo.proName]}

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Chemical Structure| 1383735-30-5
Chemical Structure| 1383735-30-5
Structure of 1383735-30-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1383735-30-5 ]

CAS No. :1383735-30-5 MDL No. :MFCD23106206
Formula : C9H9N3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 191.19 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1383735-30-5 ]

* 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 [ 1383735-30-5 ]

[ 1383735-30-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 64-17-5 ]
  • [ 201230-82-2 ]
  • [ 1150617-54-1 ]
  • [ 1383735-30-5 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine;1,1'-bis-(diphenylphosphino)ferrocene; bis(benzonitrile)palladium(II) dichloride; at 135℃; under 11251.1 Torr; for 4h; A mixture of T-7 (1.60 g, 8.08 mmol), DIPEA (2.00 mL, 11.5 mmol), dichlorobis(benzonitrile)palladium (II) (100.0 mg, 0.26 mmol), and 1,1- bis(diphenylphosphino)ferrocene (dppf) (200.0 mg, 0.36 mmol) in absolute EtOH (35 mL) in a pressure reactor is placed under 15 bars of carbon monoxide and warmed at 135C. After 4 hours, the mixture is cooled to room temperature, returned to atmospheric pressure and opened. The reaction is concentrated and then diluted with brine (100 mL) and extracted with EtOAc (3 x 75 mL). The combined organic layers are washed with brine (3 x 50 mL), dried over magnesium sulfate, treated with decolorizing carbon, filtered through filter agent and silica gel and concentrated. The residue is dissolved in DCM and passed through silica gel eluting with Et2O to provide T-8.
  • 2
  • [ 1150617-54-1 ]
  • [ 541-41-3 ]
  • [ 1383735-30-5 ]
YieldReaction ConditionsOperation in experiment
14% With n-butyllithium; In tetrahydrofuran; at -78℃; for 0.5h; Three grams <strong>[1150617-54-1]6-bromopyrazolopyridine</strong> was dissolved in 80 ml anhydrous tetrahydrofuran, 3.6 ml n-butyl lithium was added at -78 C., stirred for 5 minutes, 15 ml anhydrous tetrahydrofuran solution of ethyl chloroformate was added at -78 C., further stirred for 30 minutes. The reaction was terminated by saturated sodium bicarbonate solution, ethyl acetate was added for extraction, the organic layer was evaporated to dry, isolated by flash preparative chromatography to obtain compound 6-ethoxycarbonyl-1-H-pyrazolo[4,3-b]pyridine(m=200 mg, yield: 14%). ESI (m/z): 192.0 [M+H]+. (0577) 1H NMR (400 MHz, DMSO-d6) 9.02 (s, 1H), 8.53 (s, 1H), 8.45 (s, 1H), 4.39 (q, J=7.1 Hz, 2H), 1.37 (t, J=7.1 Hz, 3H).
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