戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1768095作成日:2026年10月26日

Rolipram → 1-(2,3-Difluorobenzyl)-4-(3-cyclopentyloxy-4-methoxyphenyl)-2-pyrrolidone

https://huagongshe.com/reaction/1768095

反応式

関与物質

役割名称HCID仕込み量
反応物RolipramHCID 5092—
反応物Ethyl AcetateHCID 8857—
反応物Sodium hydrideHCID 24758—
反応物1-(Bromomethyl)-2,3-difluoro-benzeneHCID 517984—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
溶媒15-Crown-5HCID 36336—
生成物1-(2,3-Difluorobenzyl)-4-(3-cyclopentyloxy-4-methoxyphenyl)-2-pyrrolidoneHCID 2361464770%

反応条件

温度0 °C

反応手順

4-(3-cyclopentyloxy-4-methoxyphenyl)-2-pyrrolidone (110 mg, 0.4 mmol) in 2 ml of N,N-dimethylformamide and 110 μl of 15-crown-5 is treated with sodium hydride (20 mg, 0.5 mmol) under nitrogen at ambient temperature. After 3 hours, the mixture is cooled to 0° C. and treated with 2,3-difluorobenzyl bromide (166 mg, 0.8 mmol) in 2 ml of tetrahydrofuran. The resulting mixture is allowed to stir at ambient temperature for 6 hours. 100 ml of ethyl acetate is added, followed by 100 ml of ice cold water. After usual aqueous work up, the crude product is purified by flash column chromatography (ethyl acetate/hexane 2:1) to give 112 mg (70%) of 1-(2,3-difluorobenzyl)-4-(3-cyclopentyloxy-4-methoxyphenyl)-2-pyrrolidone: 1H NMR (300 MHz, CDCl3) δ 7.18-6.98 (m, 3H), 6.79 (d, J=8.1 Hz, 1H), 6.90 (d, J=8.1 Hz, 1H), 6.68 (s, 1H) 4.71-4.69 (m, 1H), 4.60 (s, 2H), 3.81 (s, 3H), 3.68 (t, J=9.0 Hz, 1H), 3.66-3.54 (m, 1H), 3.29 (dd, J=9.6, 7.2 Hz, 1H), 2.84 (dd, J=16.8, 9.0 Hz, 1H), 2.57 (dd, J=16.8, 8.4 Hz, 1H), 2.00-1.75 (b, 6H), 1.70-1.52 (b, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07235579B2
出典データセットuspto-grants-2007_06
ORD IDord-9d4c334144084f428e3df793f6f0db78
出典メモuspto-grants-2007_06