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Chemical Structure| 886372-76-5 Chemical Structure| 886372-76-5

Structure of 886372-76-5

Chemical Structure| 886372-76-5

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Product Details of [ 886372-76-5 ]

CAS No. :886372-76-5
Formula : C7H7BrN2O3
M.W : 247.05
SMILES Code : O=[N+](C1=CC(Br)=CN=C1OCC)[O-]

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Application In Synthesis of [ 886372-76-5 ]

* 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 [ 886372-76-5 ]

[ 886372-76-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 886372-76-5 ]
  • [ 886373-00-8 ]
YieldReaction ConditionsOperation in experiment
80% To a solution of 5-bromo-2-ethoxy-3-nitropyridine (75.2 mg, 0.304 mmol) in ethyl acetate (3 mL) was added tin(II) chloride (289 mg, 1.52 mmol), and the mixture was heated to reflux for 2 h. After cooling to rt, 50% aqueous sodium hydroxide was added dropwise until a sticky brown solid completely formed. Sodium sulfate was then added, and the mixture was stirred for several minutes. The solids were then removed by filtration. The filtrate was dried over sodium sulfate, filtered, and concentrated in vacuo to provide 5-bromo-2-ethoxypyridin-3-amine (53 mg, 0.25 mmol, 80% yield) as a dark blue film. 1H NMR (400 MHz, CDCl3) delta 7.56 (d, 1H), 6.97 (d, 1H), 4.37 (q, 2H), 3.85 (br s, 2H), 1.40 (dd, 3H); MS (EI) for C7H9BrN2O: 217, 219 (Br isotopes, MH+).
79% With ammonium chloride; zinc; In methanol; dichloromethane; at 75℃; for 4h; j00144] Step 2: To a stirred solution of 5.bromo.-2-ethoxy3-nitTopyridine (1.0 equiv.) in MeOH and DCM (10:1, 0.27 M) at 25 C were added zinc (5.5 equiv.) and ammonium chloride (5.0 equiv.) and the mixture was heated to 75 C and stirred for 4 h. LCMS shows complete consumption of starting material and fairly clean conversion to a desired product (M±I=217/219, R=O.75). The reaction was cooled to room temp and filtered through a short plug of Celite, washing with DCM, and then concentrated to remove MeOH. The residue was taken up in EtOAc, washed with water and brine and then dried (MgSO1) and concentrated.The residue was quickly passed through a silica column. eluting with 0-50% EtOAc:heptanc. Product clutes around 20% EtOAc and was concentrated to give 5-bromo-2- ethoxypyridin-3-amine in 79 % yield as a light brown solid. LCMS (th) (M+H) = 217/219, Rt = 0.75 mm.
Intermediate 62 5-Bromo-2-(ethyloxy)-3-pyridinamine A solution of 5-bromo-2-(ethyloxy)-3-nitropyridine (15.5 g) in EtOAc (300 ml) was treated with tin(ll) chloride anhydrate (56.6 g) then heated at reflux for 2.5 hr. The reaction was cooled to RT then evaporated to dryness. The residue was treated with 2M NaOH (aq) (500 ml) that was treated with anhydrous magnesium sulfate (~ 50 g) then slurried to give a filterable sludge. The filtrate was separated and the organic phase was washed with brine, dried over magnesium sulfate then evaporated to dryness. The residue was purified by column chromatography on silica, eluting with DCM, to give the title compound. 1H NMR: deltaH (DMSO-d6, 400 MHz) 7.37 (1 H, d), 6.98 (1 H, d), 5.24 (2H, br.s.), 4.27 (2H, q), 1.31 (3H, t).
 

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