Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466447Generated: October 26, 2026

Potassium Carbonate → Methyl 1-{[(4'-chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetyl]amino}-4,4-difluorocyclohexanecarboxylate

https://huagongshe.com/reaction/1466447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 1-amino-4,4-difluorocyclohexanecarboxylate hydrochlorideHCID 60196672—
Reactant(4'-Chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetic acidHCID 67375533—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductMethyl 1-{[(4'-chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetyl]amino}-4,4-difluorocyclohexanecarboxylateHCID 86707849—

Reaction Conditions

Temperature80 °C

Reaction Steps

6.06 g (21.7 mmol) of the compound from Example 1A were dissolved in 7.5 ml (103 mmol) of thionyl chloride. The reaction mixture was stirred at 80° C. for 1 h and then concentrated. The residue was dissolved in 30 ml of acetonitrile. Ethyl acetate and saturated aqueous sodium bicarbonate solution were added to 5.00 g (21.8 mmol) of the compound from Example 4A. The phases were separated, the aqueous phase was extracted repeatedly with ethyl acetate and the combined organic phases were dried over sodium sulphate, filtered and concentrated. 140 ml of acetonitrile and 8.76 g (63.4 mmol) of potassium carbonate were added to the residue. With ice-cooling, the solution of the acid chloride was added dropwise, and the mixture was stirred at room temperature overnight. The mixture was then added to ice-water and extracted repeatedly with dichloromethane, and the combined organic phases were washed repeatedly with 1N aqueous hydrogen chloride solution and saturated aqueous sodium bicarbonate solution, dried over sodium sulphate, filtered and concentrated. This gave 8.22 g (83% of theory) of the title compound, which were converted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000026B2
Source datasetuspto-grants-2015_04
ORD IDord-8321529d02f4463ea5600aecd23e6157
Source noteuspto-grants-2015_04