Potassium Carbonate → 4-(6-Chloro-pyridin-2-yloxy)-1H-indole-2-carboxylic acid ethyl ester

HRID 2267899Notes

Reaction equation

HRID 2267899 reaction equation
[CH3:1][CH2:2][O:3][C:4]([C:6]1[N:7](C(OC(C)(C)C)=O)[C:8]2[C:13]([CH:14]=1)=[C:12]([OH:15])[CH:11]=[CH:10][CH:9]=2)=[O:5].[Cl:23][C:24]1[CH:29]=[CH:28][CH:27]=[C:26](Cl)[N:25]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.C(OCC)(=O)C>[CH2:2]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[C:12]([O:15][C:26]1[CH:27]=[CH:28][CH:29]=[C:24]([Cl:23])[N:25]=1)[CH:11]=[CH:10][CH:9]=2)=[O:5])[CH3:1]

Participants

6

Conditions

Temperature
160 °C

Procedure

159 (500 mg, 1.6 mmol), 2,6-Dichloro-pyridine (360 mg, 24 mmol) are dissolved in 15 ml of dimethylformamide. After addition of potassium carbonate (340 mg, 24 mmol) and a catalytic amount Cu-powder the mixture is heated to 160° C. for 3 hours. The reaction mixture is cooled to room temperature, diluted with ethyl acetate and washed with water. The organic layers are dried over sodium sulphate and evaporated. The crude product is solved in dichloromethane and after evaporation crystallized with cyclohexane.

Workup

  1. temperatureThe reaction mixture is cooled to room temperature
  2. washwashed with water
  3. dry with materialThe organic layers are dried over sodium sulphate
  4. customevaporated
  5. customafter evaporation
  6. customcrystallized with cyclohexane

Sources & evidence

ORD record
ord-0840e1713bcf4d33b01c40082b468a28
Source dataset
uspto-grants-2010_12
Patent number
US07858781B2

Reaction notes

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