Sodium Chloride → HCID 68583578, compound

HRID 645582Notes

Reaction equation

HRID 645582 reaction equation
[CH2:1]([O:3][C:4](=[O:13])[C:5]1[CH:10]=[CH:9][C:8]([F:11])=[C:7]([OH:12])[CH:6]=1)[CH3:2].[H-].[Na+].Cl[C:17]1[CH:22]=[N:21][CH:20]=[CH:19][N:18]=1.[Na+].[Cl-]>CN(C)C=O.C(O)(=O)C>[F:11][C:8]1[CH:9]=[CH:10][C:5]([C:4]([O:3][CH2:1][CH3:2])=[O:13])=[CH:6][C:7]=1[O:12][C:17]1[CH:22]=[N:21][CH:20]=[CH:19][N:18]=1

Participants

7

Conditions

Temperature
80 °C

Procedure

To a solution of 4-fluoro-3-hydroxy-benzoic acid ethyl ester (2.2 g, 11.95 mmol) in N,N-dimethylformamide (50 ml) was added 60% NaH in mineral oil (0.72 g, 17.93 mmol) and chloropyrazine (1.64 g, 14.34 mmol) and heated at 80° C. for overnight. One more equivalent of chloropyrazine was added and heated at the same temperature for 10 h. The reaction mixture was poured into a flask containing 150 ml of aqueous saturated NaCl solution and 0.6 ml of acetic acid. The mixture was extracted with ethyl acetate (3×100 ml), the combined organic extracts were washed with sat NaCl (150 ml), dried (Na2SO4), filtered and concentrated. The crude product was purified by flash column chromatography using dichloromethane to yield 1.55 g (50%) of product. MS (ESI+) m/z 263 (M+H)+;

Workup

  1. temperatureheated at the same temperature for 10 h
  2. additionThe reaction mixture was poured into a flask
  3. extractionThe mixture was extracted with ethyl acetate (3×100 ml)
  4. washthe combined organic extracts were washed with sat NaCl (150 ml)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude product was purified by flash column chromatography

Sources & evidence

ORD record
ord-349c7e135c7141daa99e15d59c1eac91
Source dataset
uspto-grants-2010_04
Patent number
US07704997B1

Reaction notes

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