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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 844229Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/844229

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-GlutamineHCID 5961—
Edukt3-Nitrophthalic anhydrideHCID 21631—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(4-Nitro-1,3-dioxoisoindolin-2-yl)-4-carbamoylbutanoic acidHCID 1554983873%

Reaktionsbedingungen

Temperatur87.5 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06380239B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-a08c992d0ecd423c89c997531ae1e485
Quellennotizuspto-grants-2002_04