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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251090Generated: November 3, 2026

Potassium Carbonate → HCID 70161506, compound

https://huagongshe.com/reaction/1251090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86757746HCID 86757746—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 70161506HCID 7016150620.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 240 mg of ethyl (Z)-[(1-{[4,4-difluoro-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepin-5-ylidene]acetyl}-4-piperidyl)-(trifluoroacetyl)amino]acetate in 5 ml of ethanol was added a solution of 100 mg of potassium carbonate in 4 ml of water, and the mixture was stirred at 40° C. for 18 hours. After evaporation of the solvent, 1N hydrochloric acid was added to the residue, and the mixture was washed with ethyl acetate. The aqueous layer was neutralized and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of NaCl and dried over anhydrous magnesium sulfate, and the solvent was evaporated therefrom. The resulting residue was crystallized from diethyl ether to give 40 mg of (Z)-[(1-{[4,4-difluoro-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepin-5-ylidene]acetyl}-4-piperidyl)amino]acetic acid as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340678B1
Source datasetuspto-grants-2002_01
ORD IDord-4f168256c82b4cbdb6e126e01d2958e7
Source noteuspto-grants-2002_01