Dimethylformamide → 6-amino-3-bromo-2-fluoro-N-methylbenzamide

HRID 2279782노트

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HRID 2279782 반응식
C1C(=O)N([Br:8])C(=O)C1.[F:9][C:10]1[C:19]2[C:18](=O)[O:17]C(=O)[NH:15][C:14]=2[CH:13]=[CH:12][CH:11]=1.CN.C1COCC1.C[N:30]([CH:32]=O)C>C(Cl)Cl.O>[NH2:15][C:14]1[C:19]([C:18]([NH:30][CH3:32])=[O:17])=[C:10]([F:9])[C:11]([Br:8])=[CH:12][CH:13]=1

참가 물질

8

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온도
0 °C

실험 절차

NBS (9.42 g, 52.9 mmol) was added to a cold (0° C.) solution of 5-fluoro-1H-benzo[d][1,3]oxazine-2,4-dione (Compound 27E, 9.2 g, 50.8 mmol) in DCM and DMF (120 mL+60 mL) over the course of 40 min. The reaction mixture was stirred at 0° C. for 2 h then allowed to warm to RT. After 30 min, the DCM was removed in vacuo. The remaining reaction mixture was cooled −10° C., treated with a solution of 2M methyl amine in THF (50.8 mL, 101.6 mmol) and allowed to stir for overnight at room temperature. The reaction mixture was poured to water (240 mL) and the resulting suspension was extracted with ethyl acetate (3×100 mL). The combined ethyl acetate layer was washed with water (3×100 mL), dried (Na2SO4) and concentrated to give crude residue which was purified by column chromatography (20% ethyl acetate/hexanes) to afford 4 g of the title compound (32% over two steps). 1H NMR (CDCl3, 500 MHz) δ=2.98 (d, J=4.5 Hz, 3H), 5.90 (brs, 2H), 6.38 (d, J=9.0 Hz, 1H), 6.55 (brs, 1H), 7.24-7.27 (m, 1H).

후처리

  1. temperatureto warm to RT
  2. waitAfter 30 min
  3. customthe DCM was removed in vacuo
  4. customThe remaining reaction mixture
  5. temperaturewas cooled −10° C.
  6. stirringto stir for overnight at room temperature
  7. extractionthe resulting suspension was extracted with ethyl acetate (3×100 mL)
  8. washThe combined ethyl acetate layer was washed with water (3×100 mL)
  9. dry with materialdried (Na2SO4)
  10. concentrationconcentrated
  11. customto give crude residue which
  12. customwas purified by column chromatography (20% ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-17356bd015694b649c48d6651cd6b31d
출처 데이터셋
uspto-grants-2015_09
특허 번호
US09133224B2

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