Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936498Generated: November 2, 2026

Sodium Hydroxide → HCID 69715313, compound

https://huagongshe.com/reaction/1936498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-[(2,6-dichlorophenyl)carbonyl]-4-[1,4-dimethyl-6-(trifluoromethyl)-2-oxo-3-pyridinyl]-L-phenylalanine methyl esterHCID 69715186—
SolventEthanolHCID 702—
ProductHCID 69715313HCID 6971531379%

Reaction Conditions

Temperature47.5 °C

Reaction Steps

To a suspension of N-[(2,6-dichlorophenyl)carbonyl]-4-[1,4-dimethyl-6-(trifluoromethyl)-2-oxo-3-pyridinyl]-L-phenylalanine methyl ester (243 mg, 0.45 mmol) in ethanol (5 mL) was added 1N aqueous sodium hydroxide solution (1.8 mL) at room temperature. The mixture was heated to 45-50° C. and was stirred for 2 h. Then, the ethanol was removed under vacuum and the residue was diluted with water (20 mL). The aqueous solution was washed with ethyl acetate (50 mL) to remove any neutral impurities. The aqueous layer was acidified with 1.0 N HCl and the product was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine solution (50 mL) and were dried over anhydrous magnesium sulfate. Filtration of the drying agent and concentration afforded 186 mg (79% yield) of N-[(2,6-dichlorophenyl)carbonyl]-4-[1,4-dimethyl-6-(trifluoromethyl)-2-oxo-3-pyridinyl]-L-phenylalanine as an amorphous white solid. ES-HRMS m/e calcd for C24H19Cl2F3N2O4 (M+Na) 549.0567, found 549.0573.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06388084B1
Source datasetuspto-grants-2002_05
ORD IDord-5a50b50a093e42e3a44c1461cf72d738
Source noteuspto-grants-2002_05