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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451168Generated: November 1, 2026

Pyridine → N-[(5-Fluoro-2-nitrophenyl)carbamoyl]glycine methyl ester

https://huagongshe.com/reaction/1451168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantHCID 53679379HCID 53679379—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductN-[(5-Fluoro-2-nitrophenyl)carbamoyl]glycine methyl esterHCID 53945193—

Reaction Steps

A solution of 5-fluoro-2-nitrobenzoyl azide (5.46 g, 0.026 mol) in toluene is stirred at 65° C. for 90 minutes, cooled, treated with glycine methyl ester hydrochloride (3.63 g, 0.029 mol), stirred for 10 minutes, treated with pyridine (5 mL, 0.062 mol), stirred overnight, diluted with water and extracted with ethyl acetate. The organic extracts are combined, washed sequentially with water, 0.4M hydrochloric acid and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a solid. The solid is slurried in an ether/hexanes (6:4) solution, filtered and dried to give a yellow solid. Column chromatography of the yellow solid using silica gel and ethyl acetate in hexanes solutions gives the title product as a yellow solid, mp 133.2°-135.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604180
Source datasetuspto-grants-1997_02
ORD IDord-69a2b4c2526d4d5398640616d859013f
Source noteuspto-grants-1997_02