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Chemical Structure| 5432-09-7 Chemical Structure| 5432-09-7

Structure of 5432-09-7

Chemical Structure| 5432-09-7

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Product Details of [ 5432-09-7 ]

CAS No. :5432-09-7
Formula : C9H7ClN2
M.W : 178.62
SMILES Code : NC1=C2N=CC=CC2=C(Cl)C=C1
MDL No. :MFCD00461243

Safety of [ 5432-09-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 5432-09-7 ]

* 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 [ 5432-09-7 ]

[ 5432-09-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6942-98-9 ]
  • [ 5432-09-7 ]
YieldReaction ConditionsOperation in experiment
82% With acetic acid; zinc; In dichloromethane; at 0℃; for 2.0h; A mixture of <strong>[6942-98-9]5-chloro-8-nitroquinoline</strong> (5 g, 23.97 mmol), and Zn (14.4 g, 239.69 mmol) in DCM (200 mL) was cooled to 0C, followed by dropwise addition of AcOH (15.7 g, 239.69 mmol). The reaction mixture was stirred at 0C for 2 hr then filtered. The filtrate was concentration under reduced pressure. The residue was purified via flash column chromatography, yielding the desired product (3.5 g, 82% yield). LC-MS: m/z 179 (M+H)+.
67% With tin(II) chloride dihdyrate; In ethanol; at 20℃; for 2.5h;Inert atmosphere; first, in 100mL two-neck eggplant type flask <strong>[6942-98-9]5-chloro-8-nitroquinoline</strong> (2.016g, 9.83mmol) was placed and dissolved in ethanol 40 mL.The reaction vessel was replaced with nitrogen and stannous (11.1 g, 49.1 mmol) chloride was added, and stirred for 2.5 hours at room temperature.Under stirring, cold water, further saturated aqueous sodium carbonate was added, basified, and separatory extraction with dichloromethane.The organic layer was concentrated with an evaporator to obtain a vacuum-dried brown solid was in a yield of 1.1 g and a yield of 67%,
10.2 g With iron; acetic acid; at 65℃; for 2.0h;Inert atmosphere; 5-Chloro-8-nitroquinoline (13.8 g, 66 mmol) was dissolved in 180 mL of acetic acid, and the ironpowder (25 g, 455 mmol) was added to the solution. The mixture was heated to 65 C for 2 h undernitrogen. The reaction was filtered through a celite pad, and washed with ethyl acetate. The filtratewas concentrated in vacuo. The resulting brown gum was dissolved in 200 mL of DCM, and basifiedby 4N NaOH aq. until pH. 10, and the solution was filtered through a celite pad, and filtrate wasextracted with DCM (3x). The combined organic layer was washed with brine and dried byanhydrous Na2SO4, and concentrated in vacuo to give 5-chloroquinolin-8-amine (10.2 g, 57 mmol,87%).
  • 2
  • [ 6942-98-9 ]
  • [ 5432-09-7 ]
  • [ 36107-01-4 ]
 

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