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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844893Generated: October 25, 2026

Water → RO-0506997

https://huagongshe.com/reaction/844893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantSodium BicarbonateHCID 516892—
ReactantCH9Z955RV6HCID 69337579—
SolventDimethylformamideHCID 6228—
ProductRO-0506997HCID 1027780093%

Reaction Steps

To a suspension of N-[(2,6-difluorophenyl)carbonyl]-4-(1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine (0.743 mmol, 340 mg) and sodium bicarbonate (5.94 mmol, 499 mg) in DMF (3.8 mL) was added iodoethane (5.94 mmol, 0.475 mL) at room temperature. The mixture was stirred for 48 h at room temperature. Then, the reaction mixture was poured into water (100 mL) and was extracted with ethyl acetate (3×25 mL). The combined extracts were washed with brine solution (80 mL) and were dried over anhydrous sodium sulfate. Filtration of the drying agent and concentration of the filtrate gave the crude product which was purified by silica gel chromatography using a Biotage (40s) column to obtain 335 mg (93% yield) of N-[(2,6-difluorophenyl)carbonyl]-4-(1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine ethyl ester as a crystalline white solid: mp 218-219° C. ES-HRMS m/e calcd for C25H25F2N3O5 (M+Na) 508.1654, found 508.1660.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380387B1
Source datasetuspto-grants-2002_04
ORD IDord-7b6e6f611f3f43eeba0ca7e37602e981
Source noteuspto-grants-2002_04