Potassium Carbonate → tert-Butyl 4-[(2-{4-[5-chloro-2-(trifluoromethoxy)phenyl]-5-methoxy-2-oxopyridin-1(2H)-yl}propanoyl)amino]benzoate

HRID 56837Notes

Reaction equation

HRID 56837 reaction equation
Br[C:2]1[C:7]([O:8][CH3:9])=[CH:6][N:5]([CH:10]([CH3:27])[C:11]([NH:13][C:14]2[CH:26]=[CH:25][C:17]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])=[CH:16][CH:15]=2)=[O:12])[C:4](=[O:28])[CH:3]=1.[Cl:29][C:30]1[CH:31]=[CH:32][C:33]([O:39][C:40]([F:43])([F:42])[F:41])=[C:34](B(O)O)[CH:35]=1.C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1>[Cl:29][C:30]1[CH:31]=[CH:32][C:33]([O:39][C:40]([F:41])([F:42])[F:43])=[C:34]([C:2]2[C:7]([O:8][CH3:9])=[CH:6][N:5]([CH:10]([CH3:27])[C:11]([NH:13][C:14]3[CH:15]=[CH:16][C:17]([C:18]([O:20][C:21]([CH3:23])([CH3:24])[CH3:22])=[O:19])=[CH:25][CH:26]=3)=[O:12])[C:4](=[O:28])[CH:3]=2)[CH:35]=1

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 53216719(5-Chloro-2-(trifluoromethoxy)phenyl)boronic acidHCID 117622877tert-Butyl 4-{[2-(4-bromo-5-methoxy-2-oxopyridin-1(2H)-yl)propanoyl]amino}benzoate

Product 1

HCID 117622758tert-Butyl 4-[(2-{4-[5-chloro-2-(trifluoromethoxy)phenyl]-5-methoxy-2-oxopyridin-1(2H)-yl}propanoyl)amino]benzoate

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

Under argon (in a flask dried by heating), 125 mg (0.28 mmol) of tert-butyl 4-{[2-(4-bromo-5-methoxy-2-oxopyridin-1(2H)-yl)propanoyl]amino}benzoate (racemate), 80 mg (0.33 mmol, 1.2 eq.) of 5-chloro-2-trifluoromethoxyphenylboronic acid, 115 mg (0.83 mmol, 3.0 eq.) of potassium carbonate and 23 mg (0.03 mmol, 0.1 eq.) of [1,1-bis(diphenylphosphino)ferrocene]palladium(II) chloride/dichloromethane monoadduct were suspended in 5.0 ml of dioxane and stirred overnight in an oil bath already preheated to 110° C. The reaction mixture was filtered through Celite and the residue was washed with dioxane. The combined filtrates were concentrated under reduced pressure. The residue was triturated with water, filtered off, washed with water and dried under reduced pressure. Yield: 155 mg (purity 83%, 82% of theory)

Workup

  1. customalready preheated to 110° C
  2. filtrationThe reaction mixture was filtered through Celite
  3. washthe residue was washed with dioxane
  4. concentrationThe combined filtrates were concentrated under reduced pressure
  5. customThe residue was triturated with water
  6. filtrationfiltered off
  7. washwashed with water
  8. customdried under reduced pressure

Sources & evidence

ORD record
ord-b2010516a0ac4e31b011154335b46ad3
Source dataset
uspto-grants-2016_09
Patent number
US09434690B2

Reaction notes

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