Tetrahydrofuran → HCID 178515146, 화합물

HRID 1987093노트

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HRID 1987093 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:12](=[O:13])[C:11]3[CH:14]=[C:15](B(O)O)[CH:16]=[CH:17][C:10]=3[CH:9]=[CH:8][C:5]2=[N:6][CH:7]=1.C1C[O:24]CC1>O.C(O)(=O)C.OO.ClCCl>[Cl:1][C:2]1[CH:3]=[C:4]2[C:12](=[O:13])[C:11]3[CH:14]=[C:15]([OH:24])[CH:16]=[CH:17][C:10]=3[CH:9]=[CH:8][C:5]2=[N:6][CH:7]=1

참가 물질

7

실험 절차

(3-chloro-5-oxo-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl)boronic acid (1.00 g, 3.5 mmol) was dissolved in a 0° C. solution of 25 mL of THF, 25 mL of water, 0.5 mL of acetic acid and 0.5 mL of 30% (w/w) hydrogen peroxide. The solution was stirred and allowed to warm to ambient temperature. After 6 h, the reaction mixture was partially concentrated and dissolved in 500 mL ethyl acetate. The organic layer was washed with water (2×100 mL), dried with magnesium sulfate, filtered, and concentrated to afford solids. The solids were dissolved in 20 mL dichloromethane and 60 mL hexanes and stirred as solids crystallized from the solution. After 2 hours, the crystalline solids were filtered and dried to afford the title compound. 1H NMR (600 MHz, DMSO-D6) δ 10.50 (s, 1H); 8.93 (s, 1H); 8.45 (s, 1H); 7.68 (d, 1H); 7.58 (d, 1H); 7.39 (d, 1H); 7.23 (d, 1H); 7.12 (d, 1H). LRMS (APCI) calculated for C14H9ClNO2 [M+H]+, 258.0; found 258.1.

후처리

  1. concentrationthe reaction mixture was partially concentrated
  2. dissolutiondissolved in 500 mL ethyl acetate
  3. washThe organic layer was washed with water (2×100 mL)
  4. dry with materialdried with magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto afford solids
  8. customcrystallized from the solution
  9. waitAfter 2 hours
  10. filtrationthe crystalline solids were filtered
  11. customdried

출처 및 근거

ORD 기록
ord-97d622526e644023ba45d6ebfaddb24c
출처 데이터셋
uspto-grants-2009_06
특허 번호
US07550478B2

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