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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381513Generated: October 29, 2026

3-[3-(3-Methyl-1-{2-[4-(3-o-tolyl-ureido)-phenyl]-acetylamino}-butyl)-isoxazol-5-yl]-propionic acid methyl ester → 3-[3-(3-Methyl-1-{2-[4-(3-o-tolyl-ureido)-phenyl]-acetylamino}-butyl)-isoxazol-5-yl]-propionic acid

https://huagongshe.com/reaction/381513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[3-(3-Methyl-1-{2-[4-(3-o-tolyl-ureido)-phenyl]-acetylamino}-butyl)-isoxazol-5-yl]-propionic acid methyl esterHCID 18682368—
Solventtert-ButanolHCID 6386—
SolventSodium HydroxideHCID 14798—
Product3-[3-(3-Methyl-1-{2-[4-(3-o-tolyl-ureido)-phenyl]-acetylamino}-butyl)-isoxazol-5-yl]-propionic acidHCID 9935407—

Reaction Steps

A mixture of 3-[3-(3-methyl-1-{2-[4-(3-o-tolyl-ureido)-phenyl]-acetylamino}butyl)-isoxazol-5-yl]-propionic acid methyl ester (17 mg) in tert-BuOH (1 ml) and 0.1 N NaOH (1 ml) was stirred at room temperature. After 20 h the mixture was concentrated under reduced pressure, dissolved in water (5 ml) and extracted with EtOAc (5 ml×3). The aqueous layer was then acidified to pH 3 with 1N HCl and extracted with EtOAc. The combined organics were washed with brine; dried over Na2SO4; filtered and concentrated under reduced pressure to give the title compound as a white amorphous solid. MP=?; MS [M+1]+ 493.2; 1H nmr (400 MHz, CD3OD) δ0.87 (d, 3H), 0.91 (d, 3H), 1.53-1.66 (m, 3H), 2.26 (s, 3H), 2.64 (t, J=7.4 Hz, 2H), 2.97 (t, J=7.5 Hz, 2H), 3.44 (s, 2H), 5.08 (m, 1H), 6.00 (s,1H), 6.99 (t, 1H), 7.11-7.36 (m, 6H), 7.59 (d, J=7.9 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306887B1
Source datasetuspto-grants-2001_10
ORD IDord-ac16e2f2b7c44527918260392d6f500f
Source noteuspto-grants-2001_10