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Chemical Structure| 105786-95-6 Chemical Structure| 105786-95-6

Structure of 105786-95-6

Chemical Structure| 105786-95-6

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Product Details of [ 105786-95-6 ]

CAS No. :105786-95-6
Formula : C6H8N2O2
M.W : 140.14
SMILES Code : [O-]C1=C2CCCC[N+]2=NO1
MDL No. :MFCD13194917

Safety of [ 105786-95-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 105786-95-6 ]

* 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 [ 105786-95-6 ]

[ 105786-95-6 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 105786-95-6 ]
  • [ 623-47-2 ]
  • [ 307307-84-2 ]
YieldReaction ConditionsOperation in experiment
56% In xylene; for 6h;Reflux; Ethyl propiolate (2.4 ml_, 23.7 mmol) was slowly added to a solution of reference example 14 (2.99 g, 21.3 mmol) in xylene (mixture of isomers, 40 ml_). The mixture was heated to reflux for 6 hours and the solvent was distilled off. The residue was purified by chromatography over silica gel using hexane/EtOAc mixtures of increasing polarity as eluent, to afford 2.3 g of the desired compound (yield: 56%). LC-MS (Method 2): tR = 1.63 min; m/z = 195 (MH+).
40.4% In 5,5-dimethyl-1,3-cyclohexadiene; at 125℃; for 12h; 4,5,6,7-tetrahydro-3-oxo-[1,2,3]oxadiazolo[3,4-a]pyridin-8-indole (17.00 g, 121.3 mmol), Xylene (80 mL) and ethyl propiolate (18.7 mL, 185 mmol) were placed in a 250 mL round bottom flask, and reacted under nitrogen for 12 h at 125 C. The reaction was complete by TLC. The mixture was spin-dried, and subjected to silica gel column chromatography, gradient elution of PE:EA=20:1-2:1 to obtain 9.52 g of a yellow liquid, the yield was 40.4%.
32% In 5,5-dimethyl-1,3-cyclohexadiene; for 2h;Reflux; General procedure: A mixture of 22a (13.0 g, 93 mmol), and ethyl propiolate (28.5 mL, 278 mmol), in xylene (250 mL) was heated under reflux for 2 h. The cooled mixture was evaporated under reduced pressure. The residual oil was purified by column chromatography (diethylether), to afford the title compound as an oil, (5.82 g, 32%). 1H NMR (CDCl3) delta: 1.39 (t, 3H), 1.88 (m, 2H), 2.06 (m, 2H), 2.82 (t, 2H), 4.20 (t, 2H), 4.39 (q, 2H), 6.55 (s, 1H). LRMS (Thermospray) m/z: 195.2 (M+1)+.
26% In o-xylene; for 16h;Heating / reflux; Step 2: 4, 5, 6, 7-TetrahYdropYrazolof1 5-alpvridine-2-carboxvlic acid ethylester :; Ethyl propiolate (804 mg) was added to the o-xylene (15 mL) solution of tetrahydropyridino [1,2-c] [1, 2,3] oxadiazolone (1.04 g) under a nitrogen atmosphere and refluxed for 16 h. The solution was concentrated under a reduced pressure. The residue was applied to silica gel column chromatography, then the column was eluted with n-hexane-AcOEt (2/1-1/1). The titled compound was obtained as yellow oil (871 mg, 65%), and 4,5, 6, 7-tetrahydropyrazolo [1,5-a] pyridine-3-carboxylic acid ethyl ester was obtained as yellow oil (345 mg, 26%). 'H NMR (CDCI3) 61. 39 (t, 3H, J = 7.1 Hz), 1.84-1. 91 (m, 2H), 2.02-2. 09 (m, 2H), 2.82 (t, 2H, J = 6.4 Hz), 4.22 (t, 2H, J = 6.2 Hz), 4.39 (q, 2H, J = 7.1 Hz), 6.53 (s, 1 H).

 

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