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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844877Generated: October 31, 2026

Sodium Hydroxide → HCID 10205401, compound

https://huagongshe.com/reaction/844877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69337249HCID 69337249—
SolventEthanolHCID 702—
ProductHCID 10205401HCID 1020540187.2%

Reaction Steps

To a suspension of N-[(2-chloro-6-methylphenyl)carbonyl]-4-(1,3-dimethyl-2,4-dioxo-5-pyrimidinyl)-3-methyl-L-phenylalanine methyl ester (0.083 mmol, 40 mg) in ethanol (1 mL) was added aqueous 1.0 N sodium hydroxide (0.2 mL) at room temperature. The mixture was stirred for 2 h at room temperature. Then, the ethanol was removed under reduced pressure and the residue was diluted with water (5 mL). The aqueous solution was washed with diethyl ether (20 mL) to remove any neutral impurities. The aqueous layer was acidified with 1.0 N HCl and the product was extracted into ethyl acetate (2×25 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 of the filtrate afforded 34 mg (87% yield) of N-[(2-chloro-6-methylphenyl)carbonyl]-4-(1,3-dimethyl-2,4-dioxo-5-pyrimidinyl)-3-methyl-L-phenylalanine as an amorphous white solid. ES-HRMS m/e calcd for C24H24ClN3O5 (M+Na) 492.1295, found 492.1301.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380387B1
Source datasetuspto-grants-2002_04
ORD IDord-076b57e68e5e484e84ec993544ccb4a0
Source noteuspto-grants-2002_04