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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844879Generated: October 30, 2026

Sodium Hydroxide → HCID 10300040, compound

https://huagongshe.com/reaction/844879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69335842HCID 69335842—
SolventEthanolHCID 702—
ProductHCID 10300040HCID 1030004041%

Reaction Steps

To a suspension of N-[(2,6-dichlorophenyl)carbonyl]-4-(1,3-dimethyl-2,4-dioxo-5-pyrimidinyl)-3-methyl-L-phenylalanine methyl ester (0.1 mmol, 59 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. The ethanol was removed under reduced pressure and the residue was diluted with water (10 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 (2×15 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 20 mg (41% yield) of N-[(2,6-dichlorophenyl)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 C23H21C2N3O5 (M+Na) 512.0752, found 512.0754.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380387B1
Source datasetuspto-grants-2002_04
ORD IDord-1bee9355fa9344c0a1510eed63b2fa31
Source noteuspto-grants-2002_04