Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60440Generated: October 25, 2026

Triethylamine → 5-Bromo-2-(3-(3-methoxy-3-oxopropyl)ureido)nicotinic acid

https://huagongshe.com/reaction/60440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantmonoMethyl succinateHCID 77487—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-Amino-5-bromonicotinic acidHCID 737445—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-(3-(3-methoxy-3-oxopropyl)ureido)nicotinic acidHCID 11887545658.9%

Reaction Steps

To a solution of 4-methoxy-4-oxobutanoic acid (14.6 g, 110.6 mmol) in toluene (530 mL) was added diphenylphosphoryl azide (30.4 g, 110.5 mmol) followed by triethylamine (18.3 g, 181.2 mmol). The reaction was stirred at RT for 30 min then 2-amino-5-bromonicotinic acid (15.9 g, 73.61 mmol) was added. The reaction was refluxed for 6 h, cooled to RT then diluted with EA (530 mL) and washed with brine (2×300 mL). The combined aqueous layers were acidified to PH 5 by adding aq. 2N HCl and a solid formed which was filtered off. The solid was dried to give 5-bromo-2-(3-(3-methoxy-3-oxopropyl)ureido)nicotinic acid (15 g, 39.3% yield) as pale yellow solid. LCMS: MH+ 347 and TR=1.047 min. Used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440972B2
Source datasetuspto-grants-2016_09
ORD IDord-8209793ed19746dea5047f1b9397dc90
Source noteuspto-grants-2016_09