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[ CAS No. 26956-43-4 ] {[proInfo.proName]}

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Chemical Structure| 26956-43-4
Chemical Structure| 26956-43-4
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Product Details of [ 26956-43-4 ]

CAS No. :26956-43-4 MDL No. :MFCD00183939
Formula : C7H5NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :FYNCIYHECMWXPK-UHFFFAOYSA-N
M.W : 135.12 Pubchem ID :288746
Synonyms :

Safety of [ 26956-43-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H320-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 26956-43-4 ]

* 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 [ 26956-43-4 ]

[ 26956-43-4 ] Synthesis Path-Downstream   1~13

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YieldReaction ConditionsOperation in experiment
81% Reference Example 4 4-chlorofuro[3,2-c]pyridine; [Show Image] <strong>[26956-43-4]Furo[3,2-c]pyridin-4(5H)-one</strong> (72.2 g, 534 mmol) was added to phosphorus oxychloride (100 mL) heated to 120C, and the mixture was stirred for 30 min. The solvent was evaporated under reduced pressure. Ice-cooled water was added to the residue, and the mixture was basified with 8M aqueous sodium hydroxide solution and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=30/70) to give the title compound (66.1 g, yield 81%). 1H-NMR (CDCl3) delta: 7.13 (1H, dd, J = 2.2, 1.0 Hz), 7.79 (1H, dd, J = 5.8, 1.0 Hz), 8.27 (1H, d, J = 2.2 Hz), 8.32 (1H, d, J = 5.8 Hz).
With trichlorophosphate; at 120℃; for 3h; 5H-Furo [3,2-c] pyridin-4-one (5.9 g) was suspended with POCI3 (12 ml) and the reaction mixture was stirred for 3 hours at 120 C. After evaporating POCI3, crushed ice was added and poured into the mixture of ethyl acetate and saturated NaHCO3. The corresponding organic phase was separated and dried over NA2SO4 and then concentrated in vacuo. The resultant residue was purified by chromatography on a silica gel column to afford 4-chloro-furo [3,2-c] pyridine (5.6 g) 1 H NMR (400MHZ, DMSO-D6) ppm 8.31 (d, J = 5.8Hz, 1H), 8.26 (d, J = 2.3Hz, 1H), 7.79 (dd, J = 1.0, 5.6 Hz, 1H), 7.13 (dd, J=1.0, 2.3 Hz, 1 H).
With trichlorophosphate; In acetonitrile; at 110℃; for 0.0833333h;Microwave irradiation; General procedure: A solution of 6,7-dimethoxyisoquinolin-1(2H)-one(200 mg, 0.97 mmol), phosphoryl trichloride (0.268 mL, 2.92 mmol) inacetonitrile (5 mL) was stirred at 110 C for 5 minutes under microwaveirradiation. The reaction was quenched with a saturated aqueous sodium bicarbonatesolution and stirred at ambient temperature for 1 h. It was filtered throughcelite and washed with ethyl acetate. The filtrate was concentrated to dryness.The crude material was purified by flash chromatography, eluting with heptanesand ethyl acetate (1:0 to 0:1) to give the desired product as a gum (99 mg,45.4 %).
With trichlorophosphate; for 3h;Heating / reflux; [0155] Furopyridone (6,3. 26 g, 24.15 mmol) is treated with phosphorus oxychloride (10 ml) at refluxing temperature for 3 hours. After cooling, the dark solution is poured into ice and basified with aqueous sodium hydroxide to pH-9. The mixture is extracted with chloroform. After evaporation of the chloroform, the brown oil is applied to flash column chromatography on silica gel to give chlorofuropyridine as yellow crystalline solid (7).
With trichlorophosphate; at 120 - 140℃; for 2.5h; Next, Compound (3) (60.0 g, 444 mmol) and phosphorus oxychloride (POCl3) (62 mL, 666 mmol) were added into a reaction bottle. After heating the reaction bottle to 120-140 C. for 2.5 hours, the reaction bottle was cooled to 25 C. The reaction was quenched by water under ice bath. Next, the reaction mixture was neutralized with sodium hydroxide. The mixture was extracted with ethyl acetate (EA) and water. Next, an organic phase was separated and concentrated. Next, after removing water and concentrating, the result was purified by column chromatography. Compound (4) was obtained. The synthesis pathway of the above reaction was as follows:

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YieldReaction ConditionsOperation in experiment
With tributyl-amine; In diphenylether; at 230℃; for 0.5h; Next, tri-n-butylamine ((nBu)3N) (41.3 ml, 500 mmol) and diphenyl ether (21.7 ml) were added into a reaction bottle. Next, after heating the reaction bottle to 230 C., Compound (2) (40.8 g, 250 mmol) (dissolved in 217 ml of diphenyl ether) was slowly added into the reaction bottle. After reacting for half hour, n-hexane was added into the reaction bottle. After filtrating and collecting the solid, Compound (3) was obtained. The synthesis pathway of the above reaction was as follows:
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  • 4-(1-cyanoethoxy)furo<3,2-c>pyridine [ No CAS ]
  • (1R*,2aS*,7bS*)-1-cyano-4-oxo-1,2,2a,3,4,7b-hexahydrocyclobuta<g>furo<3,2-c>pyridine [ No CAS ]
  • (2S*,2aR*,7bR*)-2-cyano-4-oxo-1,2,2a,3,4,7b-hexahydrocyclobuta<g>furo<3,2-c>pyridine [ No CAS ]
  • (2R*,2aR*,7bR*)-2-cyano-3-methyl-4-oxo-1,2,2a,3,4,7b-hexahydrocyclobuta<g>furo<3,2-c>pyridine [ No CAS ]
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  • 4-(1-cyanoethoxy)furo<3,2-c>pyridine [ No CAS ]
  • (1S*,2aS*,7bS*)-1-cyano-4-oxo-1,2,2a,3,4,7b-hexahydrocyclobuta<g>furo<3,2-c>pyridine [ No CAS ]
  • (1R*,2aS*,7bS*)-1-cyano-4-oxo-1,2,2a,3,4,7b-hexahydrocyclobuta<g>furo<3,2-c>pyridine [ No CAS ]
  • (2S*,2aR*,7bR*)-2-cyano-4-oxo-1,2,2a,3,4,7b-hexahydrocyclobuta<g>furo<3,2-c>pyridine [ No CAS ]
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  • 4-(1-cyanoethoxy)furo<3,2-c>pyridine [ No CAS ]
  • (1R*,2aS*,7bS*)-1-cyano-4-oxo-1,2,2a,3,4,7b-hexahydrocyclobuta<g>furo<3,2-c>pyridine [ No CAS ]
  • (2S,2aR,7bS)-4-Oxo-1,2,2a,3,4,7b-hexahydro-7-oxa-3-aza-cyclobuta[e]indene-2-carbonitrile [ No CAS ]
  • (2S*,2aR*,7bR*)-2-cyano-4-oxo-1,2,2a,3,4,7b-hexahydrocyclobuta<g>furo<3,2-c>pyridine [ No CAS ]
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