Potassium Carbonate → HCID 28254339, compound

HRID 1023521Notes

Reaction equation

HRID 1023521 reaction equation
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.[CH3:11][CH:12]([C:14]1[CH:15]=[C:16]([OH:20])[CH:17]=[CH:18][CH:19]=1)[CH3:13].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH3:11][CH:12]([C:14]1[CH:15]=[C:16]([O:20][C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=2)[CH:17]=[CH:18][CH:19]=1)[CH3:13]

Participants

5

Conditions

Temperature
110 °C

Procedure

In a 30 mL large microwave vial, 2-chloro-5-nitropyridine (1.041 g, 6.57 mmol, 1 equiv) was dissolved in 5.5 mL of dimethylformamide. 3-(1-methylethyl)phenol (0.90 mL, 6.57 mmol, 1 equiv) and potassium carbonate (4.54 g, 32.8 mmol, 5 equiv) were added. The reaction mixture was heated under microwave irradiation for 1 hour at 110° C. (Biotage Initiator). The reaction mixture was filtered. The filtrated solid was washed with dichloromethane (30 mL). The volatiles were evaporated under vacuum. The crude compound was dissolved in dichoromethane (20 mL) and brine was added (20 mL). The compound was extracted 2 times with dichloromethane (2×20 mL) and 2 times with ethyl acetate (2×20 mL). The organic phase was dried over sodium sulphate. Evaporation afforded the title compound (1.402 g).

Workup

  1. filtrationThe reaction mixture was filtered
  2. washThe filtrated solid was washed with dichloromethane (30 mL)
  3. customThe volatiles were evaporated under vacuum
  4. dissolutionThe crude compound was dissolved in dichoromethane (20 mL)
  5. additionbrine was added (20 mL)
  6. extractionThe compound was extracted 2 times with dichloromethane (2×20 mL) and 2 times with ethyl acetate (2×20 mL)
  7. dry with materialThe organic phase was dried over sodium sulphate
  8. customEvaporation

Sources & evidence

ORD record
ord-b1312467dc74472bb4c9d8df85791c4f
Source dataset
uspto-grants-2014_05
Patent number
US08722695B2

Reaction notes

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