Anthranilic Acid → 2-(3-chlorophenylamino)-6-octyl-4H-3,1-benzoxazin-4-one

HRID 430949

반응식

HRID 430949 반응식
[C:1]([OH:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[Cl:11][C:12]1[CH:13]=[C:14]([N:18]=[C:19]=O)[CH:15]=[CH:16][CH:17]=1.O1[C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=2[CH2:24][C:23](=O)N1.NC(N)=O>C1COCC1>[Cl:11][C:12]1[CH:13]=[C:14]([NH:18][C:19]2[O:9][C:1](=[O:10])[C:2]3[CH:8]=[C:7]([CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH:6]=[CH:5][C:3]=3[N:4]=2)[CH:15]=[CH:16][CH:17]=1

참가 물질

6

실험 절차

The anthranilic acid (200 mg, 0.8 mmol) was dissolved in anhydrous THF (1 ml), and to this was added 3-chlorophenylisocyanate (117 μl, 0.96 mmol). The mixture was stirred for 3 h before being concentrated. The residue was partitioned between water and ethyl acetate. The organic layer was washed with 5% aqueous citric acid, saturated aqueous sodium bicarbonate and brine then dried (MgSO4) and concentrated to give an orange solid. This was purified by flash chromatography on silica (15% EtOAc/hexane to 100% EtOAc, then 10% EtOH/EtOAc) which gave, in order of elution, the benzoxazinone (18 mg, 0.05 mmol); δH (400 MHz, CDCl3) 0.77-0.82 (3H, m, Me), 1.19-1.24 (10H, m, 5×CH2), 1.55-1.57 (2H, m, ArCH2CH2), 2.56-2.62 (2H, m, ArCH2), 7.00-7.32 (4H, m, 3×ArH, NH), 7.40-7.49 (2H, m, 2×ArH), 7.81-7.83 (2H, m, ArH); m/z (ES+) 385 (MH+) and the urea (160 mg, 0.4 mmol); m/z (ES−) 401 (M−H)−.

후처리

  1. concentrationbefore being concentrated
  2. customThe residue was partitioned between water and ethyl acetate
  3. washThe organic layer was washed with 5% aqueous citric acid, saturated aqueous sodium bicarbonate and brine
  4. dry with materialthen dried (MgSO4)
  5. concentrationconcentrated
  6. customto give an orange solid
  7. customThis was purified by flash chromatography on silica (15% EtOAc/hexane to 100% EtOAc
  8. custom10% EtOH/EtOAc) which gave, in order of elution

출처 및 근거

ORD 기록
ord-4003d3bed4964987a4570d398919c426
출처 데이터셋
uspto-grants-2003_12
특허 번호
US06656934B2

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