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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844863Generated: October 30, 2026

Sodium Hydroxide → HCID 69336100, compound

https://huagongshe.com/reaction/844863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69336818HCID 69336818—
SolventEthanolHCID 702—
ProductHCID 69336100HCID 6933610080.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of N-[(2,6-dichlorophenyl)carbonyl]-4-(1,3-diethyl-6-methyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine methyl ester (0.77 mmol, 0.41 g) in ethanol (2 mL) was added aqueous 1.0 N sodium hydroxide (1.5 mL) at room temperature. The mixture was heated to 50° C. and the resulting clear solution was stirred for 2 h. Then, the ethanol was removed under reduced pressure and the residue was diluted with water (25 mL) and NaOH (2 mL, 1.0N) to dissolve the sodium salt. The aqueous solution was washed with diethyl ether (30 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 320 mg (80% yield) of N-[(2,6-dichlorophenyl)carbonyl]-4-(1,3-diethyl-6-methyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine as an amorphous white solid. ES-HRMS m/e calcd for C25H25Cl2N3O5 (M+Na) 541.3921, found 541.3925.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380387B1
Source datasetuspto-grants-2002_04
ORD IDord-3dbe1552a00645e5ba082b69cb82c9d2
Source noteuspto-grants-2002_04