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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-[3-(3-Methyl-1-{2-[4-(3-o-tolyl-ureido)-phenyl]-acetylamino}-butyl)-isoxazol-5-yl]-propionic acid methyl ester | HCID 18682368 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-[3-(3-Methyl-1-{2-[4-(3-o-tolyl-ureido)-phenyl]-acetylamino}-butyl)-isoxazol-5-yl]-propionic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06306887B1 |
|---|
| Source dataset | uspto-grants-2001_10 |
|---|
| ORD ID | ord-ac16e2f2b7c44527918260392d6f500f |
|---|
| Source note | uspto-grants-2001_10 |
|---|