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Chemical Structure| 16101-63-6 Chemical Structure| 16101-63-6

Structure of 16101-63-6

Chemical Structure| 16101-63-6

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Product Details of [ 16101-63-6 ]

CAS No. :16101-63-6
Formula : C11H11NO3
M.W : 205.21
SMILES Code : O=C1NC=CC2=C1C=C(OC)C(OC)=C2
MDL No. :MFCD00086979

Safety of [ 16101-63-6 ]

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

Application In Synthesis of [ 16101-63-6 ]

* 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 [ 16101-63-6 ]

[ 16101-63-6 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 16101-63-6 ]
  • [ 21560-29-2 ]
YieldReaction ConditionsOperation in experiment
45.4% With trichlorophosphate; In acetonitrile; at 110℃; for 0.0833333h;Microwave irradiation; A solution of 6,7-dimethoxyisoquinolin-1(2H)-one(200 mg, 0.97 mmol), phosphoryl trichloride (0.268 mL, 2.92 mmol) in acetonitrile (5 mL) was stirred at 110C for 5 minutes under microwave irradiation. The reaction was quenched with a saturated aqueous sodium bicarbonate solution and stirred at ambient temperature for 1 h. It was filtered through celite and washed with ethyl acetate. The filtrate was concentrated to dryness.The crude material was purified by flash chromatography, eluting with heptanes and ethyl acetate (1:0 to 0:1) to give the desired product as a gum (99 mg,45.4 %). MS m/z 224.0 [M+H]+ (ESI).
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 %).
 

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