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Chemical Structure| 74696-96-1 Chemical Structure| 74696-96-1

Structure of 74696-96-1

Chemical Structure| 74696-96-1

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Product Details of [ 74696-96-1 ]

CAS No. :74696-96-1
Formula : C15H17NO3
M.W : 259.30
SMILES Code : O=C1C(C(C)=O)=CC2=C(O1)C=C(N(CC)CC)C=C2
MDL No. :MFCD00068687
InChI Key :JQYDECSZBZCKFQ-UHFFFAOYSA-N
Pubchem ID :688763

Safety of [ 74696-96-1 ]

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 [ 74696-96-1 ]

* 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 [ 74696-96-1 ]

[ 74696-96-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 25475-67-6 ]
  • [ 74696-96-1 ]
  • 7-(diethylamino)-3-(imidazo[1,2-b]isoquinolin-2-yl)-2H-chromen-2-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
67.3% (1.0 mmol, 0.259 g) 3-acetyl-7-diethylaminocoumarin, (1.4 mmol, 0.202 g) of <strong>[25475-67-6]3-aminoisoquinoline</strong>, and (1.0 mmol, 0.254 g) were added to a 50 mL pear-shaped flask. Iodine is used as a catalyst. The mixture in the pear-shaped bottle was stirred at 110 C for 4 h.Cool to 70 C and stir overnight. Then add 5 mL of distilled water and 0.6 mL of mass fraction45% sodium hydroxide solution (adjusted solution pH 12), the mixture was stirred at 100 C for 1 h, cooled to room temperature, and added to 0.3 mL of 10% dilute hydrochloric acid to neutralize until neutral The solution. Extract 3 times with dichloromethane (25 mL each time), combine the extracts, dry over anhydrous sodium sulfate, concentrate and remove the solvent, then use column chromatography (eluent: V ethyl acetate / V petroleum ether = 1:4) 7-Diethylamino-3-(2-imidazo[1,2b]isoquinoline)-coumarin (abbreviated as NQ) yellow solid product (0.258 g, yield 67.3%) was isolated.
39% With iodine; In neat (no solvent); at 80 - 110℃; for 14h; General procedure: A mixture of 2a (0.92 mmol, 0.1740 g), 2-aminopyridine(2.1 mmol, 0.1974 g) and iodine (1.0 mmol, 0.254 g) was stirred for2 h at 110 C, and then stirred for another 12 h at 80 C. The residue was diluted with 2mL of distilled water and added excess of 0.1mL aqueous sodium hydroxide (45%). Then the reaction mixture was stirred at 100 C for 30 min. After cooling to room temperature, the reaction mixture was diluted with 25 mL DCM and added 10% aqueous HCl to the mixture until a neutral pH. The mixture was then extracted with DCM (30 mL 3), and the organic layer was washed with water, and dried with Na2SO4, and concentrated under reduced pressure. The solid was isolated by column chromatography(silica, ethyl acetate/petroleum ether 1:1 todichloromethane/petroleum ether 3:1) to afford dark yellow solid3-HP (0.1063 g, 43%).
 

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