Ethyl (6-bromo-2-nitropyridin-3-yloxy)acetate → 6-Bromo-2H-pyrido[3,2-B][1,4]oxazin-3(4H)-one

HRID 1435855Notes

Reaction equation

HRID 1435855 reaction equation
[Br:1][C:2]1[N:7]=[C:6]([N+:8]([O-])=O)[C:5]([O:11][CH2:12][C:13]([O:15]CC)=O)=[CH:4][CH:3]=1>CC(O)=O.CCOC(C)=O.C(Cl)(Cl)Cl.[Fe]>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[O:11][CH2:12][C:13](=[O:15])[NH:8][C:6]=2[N:7]=1

Participants

5

Conditions

Temperature
77 °C

Procedure

Ethyl (6-bromo-2-nitropyridin-3-yloxy)acetate (41 g, 0.132 mole) was dissolved in glacial AcOH (400 mL) and the solution was heated to 77° C. with mechanical stirring. Iron powder (50 g, 0.89 mole) was added portionwise over 2 hr, so that the temperature did not rise above 90° C. The mixture was mechanically stirred and heated at 77° C. for 10 hr then was cooled to room temperature and diluted with 1:4 EtOAc/CHCl3 (1 L). The mixture was filtered through a pad of celite® and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography on silica gel (1 kg; 0-10% EtOAc/CHCl3) to afford the title compound (21.5 g, 70%): MS (ES) m/e 229 (M+H)+.

Workup

  1. customdid not rise above 90° C
  2. temperatureheated at 77° C. for 10 hr
  3. temperaturethen was cooled to room temperature
  4. filtrationThe mixture was filtered through a pad of celite®
  5. concentrationthe filtrate was concentrated in vacuo
  6. customThe residue was purified by flash chromatography on silica gel (1 kg; 0-10% EtOAc/CHCl3)

Sources & evidence

ORD record
ord-996e451e655c44979c633322572d88ec
Source dataset
uspto-grants-2009_11
Patent number
US07618959B2

Reaction notes

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