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HRID 1940057作成日:2026年10月25日

Ammonium Hydroxide → 2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-phenylpropanamide

https://huagongshe.com/reaction/1940057

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物N-Phthaloyl-DL-phenylalanineHCID 227754—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-phenylpropanamideHCID 363234084%

反応手順

To a stirred solution of 2-phthalimido-3-phenylpropionic acid (2.95 g, 10.0 mmol) in tetrahydrofuran (25 mL) are added carbonyldiimidazole (1.62 g, 10.0 mmol) and a few crystals of 4-N,N-dimethylaminopyridine, followed by 15 mL of tetrahydrofuran. The reaction mixture is stirred at room temperature for 45 minutes and 1 mL of concentrated ammonium hydroxide then is added. After 10 minutes, the reaction mixture is diluted with 50 mL water and the resulting slurry is partially concentrated to remove the tetrahydrofuran and filtered. The solid is washed with water and dried in vacuo (60° C., <1 mm) to afford 2.46 g (84%) of 2-phthalimido-3-phenylpropionamide as a white powder: mp 224°-226° C.; 1H NMR (DMSO-d6, 250 MHz) δ7.79 (s, 4H, Ar), 7.71 (br s, 1H, CONH2), 7.32 (br s, 1H, CONH2), 7.20-7.02 (m, 5H, Ar), 5.06-4.98 (m, 1H), 3.56-325 (m 2H); 13C NMR (DMSO-d6, 250 MHz)d: 169.6, 168.0, 137,1, 134.3, 131.2, 129.5, 128.1, 126.3, 122.9, 54.2, 33.7. Anal. Calculated for C17H14N2O3. Theoretical: C, 69.38; H,4.79; N, 9.52. Found: C, 69.37; H, 4.73; N, 9.43.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05698579
出典データセットuspto-grants-1997_12
ORD IDord-8d21e6ab8ec94c7187841cfca1ffb49e
出典メモuspto-grants-1997_12