Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844229Generated: October 26, 2026

L-Glutamine → 2-(4-Nitro-1,3-dioxoisoindolin-2-yl)-4-carbamoylbutanoic acid

https://huagongshe.com/reaction/844229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-GlutamineHCID 5961—
Reactant3-Nitrophthalic anhydrideHCID 21631—
SolventDimethylformamideHCID 6228—
Product2-(4-Nitro-1,3-dioxoisoindolin-2-yl)-4-carbamoylbutanoic acidHCID 1554983873%

Reaction Conditions

Temperature87.5 °C

Reaction Steps

A mixture of 3-nitrophthalic anhydride (1.5 g, 7.8 mmol) and L-glutamine (1.14 g, 7.8 mmol) in DMF (15 mL) is heated at 85-90° C. for 4 hours. The mixture is concentrated in vacuo and the residue is slurried with water (30 mL). The resulting slurry is filtered and the solid is washed with water (10 mL), dried (60° C., <1 mm Hg) to give 2-(4-nitro-1,3-dioxoisoindolin-2-yl)-4-carbamoylbutanoic acid (1.82 g, 73%); mp 182-184° C.; 1H NMR (DMSO-d6) δ8.33 (d, J=7.7 Hz, 1H), 8.22 (d, J=7.0 Hz, 1H), 8.11 (t, J=7.8 Hz, 1H), 7.19 (s, 1H), 6.73 (s, 1H), 4.82-4.77 (dd, J=4.6 and 9.8 Hz, 1H), 2.36-2.11 (m, 4H); 13C NMR (DMSO-d6) δ173.21, 170.03, 165.43, 162.75, 144.45, 136.70, 132.98, 128.83, 127.25, 122.52, 51.87, 31.31, 23.87; Anal. Calcd. For C13H11N3O7: C, 48.60; H, 3.45; N, 13.08. Found: C, 48.52; H, 3.28; N, 13.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380239B1
Source datasetuspto-grants-2002_04
ORD IDord-a08c992d0ecd423c89c997531ae1e485
Source noteuspto-grants-2002_04