Potassium Iodide → Quinoline-6-carboxylic acid oxiranylmethyl ester

HRID 720882Notes

Reaction equation

HRID 720882 reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([OH:13])=[O:12])=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH2:14]([CH:16]1[O:18][CH2:17]1)Cl.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CN(C=O)C>[O:18]1[CH2:17][CH:16]1[CH2:14][O:12][C:11]([C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[N:1]=[CH:2][CH:3]=[CH:4]2)=[O:13]

Participants

6

Procedure

Quinoline-6-carboxylic acid (1 g; 5.78 mmol) is dissolved in DMF (10 mL) at ambient temperature. Epichlorohydrin (0.4517 mL; 5.59 mmol) is added followed by mortar ground potassium carbonate (0.80 g; 5.79 mmol). The mixture is stirred at ambient temperature for 48 hours. Potassium iodide (96 mg; 0.58 mmol) is added and stirring is continued at ambient temperature for 24 hours. The mixture is heated to 60° C. and maintained for 72 hours. After cooling, the mixture is poured onto water (700 mL) and extracted with ethyl acetate (3×100 mL). The combined organic extracts are washed successively with water (100 mL), and brine (50 mL), then dried over MgSO4, filtered, and concentrated in vacuo at 30 C. The residue is purified via silica gel chromatography with gradient elution (20%→67% ethyl acetate in hexanes) affording the desired product (270 mg) as a white solid. ESMS:MH+ 230.0 (base).

Workup

  1. stirringstirring
  2. waitis continued at ambient temperature for 24 hours
  3. temperatureThe mixture is heated to 60° C.
  4. temperaturemaintained for 72 hours
  5. temperatureAfter cooling
  6. additionthe mixture is poured onto water (700 mL)
  7. extractionextracted with ethyl acetate (3×100 mL)
  8. washThe combined organic extracts are washed successively with water (100 mL), and brine (50 mL)
  9. dry with materialdried over MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo at 30 C
  12. customThe residue is purified via silica gel chromatography with gradient elution (20%→67% ethyl acetate in hexanes)

Sources & evidence

ORD record
ord-c597ed8ffc5440bfb0bf63008421358f
Source dataset
uspto-grants-2006_11
Patent number
US07135483B2

Reaction notes

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