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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433666Generated: October 28, 2026

Triethylamine → 2-Tert-butoxycarbonylamino-3-[3-(1-{[4-(3-o-tolyl-ureido)-phenyl]-acetyl}-pyrrolidin-2-yl)-isoxazol-5-yl]-propionic acid methyl ester

https://huagongshe.com/reaction/433666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 2-[(tert-butoxycarbonyl)amino]pent-4-ynoateHCID 10537281—
ReactantSodium HypochloriteHCID 23665760—
Reactant1-(4-{2-[2-(Hydroxyimino-methyl)-pyrrolidin-1-yl]-2-oxo-ethyl}-phenyl)-3-o-tolyl-ureaHCID 87972858—
SolventDichloromethaneHCID 6344—
Product2-Tert-butoxycarbonylamino-3-[3-(1-{[4-(3-o-tolyl-ureido)-phenyl]-acetyl}-pyrrolidin-2-yl)-isoxazol-5-yl]-propionic acid methyl esterHCID 2061030414%

Reaction Steps

A solution of 1-(4-{2-[2-(hydroxyimino-methyl)-pyrrolidin-1-yl]-2-oxo-ethyl}-phenyl)-3-o-tolyl-urea (300 mg, 0.789 mmol), 2-tert-butoxycarbonylamino-pent-4-ynoic acid methyl ester (359 mg, 1.182 mmol, crude mixture) and triethyl amine (12.9 μL) in dichloromethane (2 mL) was stirred 5 minutes. A sodium hypochlorite solution (5.25%, 2 mL) was added. The reaction was stirred at room temperature overnight. The aqueous portion was extracted 4 times with dichloromethane. The combined organic portions were washed with brine, dried over magnesium sulfate and concentrated. Chromatography of the crude mixture on a Biotage Flash 40S column eluting with ethyl acetate/hexane 1:5 gave the title compound (66 mg, 14%). MS (CI) m/z 604.5 (M−1), 505.9 (M-99)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667331B2
Source datasetuspto-grants-2003_12
ORD IDord-5fe9ca639e4f4fc382497bdf18fb5f5c
Source noteuspto-grants-2003_12