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HRID 844229作成日:2026年10月26日

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

https://huagongshe.com/reaction/844229

反応式

関与物質

役割名称HCID仕込み量
反応物L-GlutamineHCID 5961—
反応物3-Nitrophthalic anhydrideHCID 21631—
溶媒DimethylformamideHCID 6228—
生成物2-(4-Nitro-1,3-dioxoisoindolin-2-yl)-4-carbamoylbutanoic acidHCID 1554983873%

反応条件

温度87.5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06380239B1
出典データセットuspto-grants-2002_04
ORD IDord-a08c992d0ecd423c89c997531ae1e485
出典メモuspto-grants-2002_04