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Chemical Structure| 17965-74-1 Chemical Structure| 17965-74-1

Structure of 17965-74-1

Chemical Structure| 17965-74-1

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Product Details of [ 17965-74-1 ]

CAS No. :17965-74-1
Formula : C8H5BrN2
M.W : 209.04
SMILES Code : BrC1=C2N=CC=CC2=CN=C1
MDL No. :MFCD00234384
InChI Key :PQBNZTONCGWKCZ-UHFFFAOYSA-N
Pubchem ID :817270

Safety of [ 17965-74-1 ]

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

Application In Synthesis of [ 17965-74-1 ]

* 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 [ 17965-74-1 ]

[ 17965-74-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 253-72-5 ]
  • [ 17965-74-1 ]
YieldReaction ConditionsOperation in experiment
68% With bromine; acetic acid; at 80℃; To the solution of <strong>[253-72-5]1,6-naphthyridine</strong> (830 mg, 6.38 mmol) in HOAc (5 mL), was added dropwise dibromine (612 mg, 3.83 mmol). The resulting suspension was stirred at 80°C overnight. The reaction mixture was cooled to room temperature and added saturated NaHCC>3 aqueous solution to adjust pH to 8, extracted with dichloromethane (100 mL x 3). The combined organic layer was evaporated. The residue was purified by silica gel column chromatography (petroleum ether/ethyl acetate = 1/1) to give the desired product (700 mg, 68percent) as a pale solid. H NMR (400 MHz, CDC13) delta 9.24 (d, / = 2.8 Hz, 1H), 9.21 (s, 1H), 9.02 (s, 1H), 8.34 (d, / = 8.0 Hz, 1H), 7.64 (dd, / = 8.0, 4.0 Hz, 1H).
27% To a stirred solution of <strong>[253-72-5][1,6]-naphthyridine</strong> (4.73 g, 36.4 mmol) in CCl4 (200 mL) was added Br2 (2.25 mL, 43.7 mmol) in CCl4 (35 mL) dropwise via an addition funnel. The resulting solution was heated at reflux for 1 hour. Pyridine (2.94 mL, 36.4 mmol) in CCl4 (30 mL) was added dropwise to the refluxing solution, and the mixture was refluxed overnight. The cooled reaction mixture was filtered, and the solids were digested with 1 M NaOH (200 mL) for 1 hour. The basic solution was extracted into CH2Cl2 (2 x 200 mL), and the organic fractions were combined, dried over Na2SO4 and concentrated. The resulting oil was purified by column chromatography (10percent EtOAc/CH2Cl2) affording 2.03 g (27percent) of the title compound as yellow crystals: mp 79-81 °
 

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