Methyl iodide → 5-chloro-6-fluoro-1-methyl-1H-benzo[d][1,3]oxazine-2,4-dione

HRID 2244371노트

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HRID 2244371 반응식
[H-].[Na+].[Cl:3][C:4]1[C:13]2[C:12](=[O:14])[O:11][C:10](=[O:15])[NH:9][C:8]=2[CH:7]=[CH:6][C:5]=1[F:16].[CH3:17]I>CN(C=O)C>[Cl:3][C:4]1[C:13]2[C:12](=[O:14])[O:11][C:10](=[O:15])[N:9]([CH3:17])[C:8]=2[CH:7]=[CH:6][C:5]=1[F:16]

참가 물질

5

실험 절차

To a suspension of NaH (49 mg, 1.11 mmol) in DMF (2 ml) at RT was added a solution of 5-chloro-6-fluoro-1H-benzo[d][1,3]oxazine-2,4-dione (synthesized in analogy to a procedure described in EP 59391) (200 mg, 0.93 mmol) in DMF (2 ml). The mixture was stirred at RT for 1 h and then methyl iodide (87 μl, 1.39 mmol) was added. The reaction mixture was then warmed up to RT and stirring was continued overnight. The mixture was quenched with water and extracted with ether. The organic phase was washed with water and brine, dried (MgSO4), filtered, and concentrated in vacuo to give a residue which was purified by flash column chromatography (1:1 ethyl acetate:cyclohexane) to give the desired compound (83 mg, 39%) as a light yellow solid. 1H NMR (CDCl3, 300 MHz): 7.56 (dd, J=9.5, 8.0 Hz, 1H), 7.10 (dd, J=9.5, 4.0 Hz, 1H), 3.59 (s, 3H).

후처리

  1. customsynthesized in analogy to a procedure
  2. temperatureThe reaction mixture was then warmed up to RT
  3. stirringstirring
  4. waitwas continued overnight
  5. customThe mixture was quenched with water
  6. extractionextracted with ether
  7. washThe organic phase was washed with water and brine
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. customto give a residue which
  12. customwas purified by flash column chromatography (1:1 ethyl acetate:cyclohexane)

출처 및 근거

ORD 기록
ord-37a28c7c943a47a3b72da1e917a5277a
출처 데이터셋
uspto-grants-2010_03
특허 번호
US07678818B2

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