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HRID 522361作成日:2026年10月25日

Pyridine → 1-[({[(1R,2R)-2-(pent-4-yn-1-yl)cyclopropyl]oxy}carbonyl)oxy]pyrrolidine-2,5-dione

https://huagongshe.com/reaction/522361

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Di(succinimido) carbonateHCID 676246—
反応物rel-(1R,2R)-2-(pent-4-en-1-yl)cyclopropan-1-olHCID 67304189—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Diethyl EtherHCID 3283—
溶媒AcetonitrileHCID 6342—
生成物1-[({[(1R,2R)-2-(pent-4-yn-1-yl)cyclopropyl]oxy}carbonyl)oxy]pyrrolidine-2,5-dioneHCID 89590835—

反応条件

温度40 °C

反応手順

To a solution of (1R,2R)-2-(pent-4-en-1-yl)cyclopropanol (See International Patent Application Publication No. WO08/057209) (2.13 g; 70% wt) in acetonitrile (20 ml) was added pyridine (1.5 ml), followed by N,N′-disuccinimidyl carbonate (3.74 g) and a crystal of DMAP. The mixture was stirred at 40° C. overnight. After cooling to room temperature, the reaction mixture was diluted with ether and washed with HCl 1N, water and brine and dried over sodium sulfate. The organic layer was filtered and concentrated to provide the desired product (2.88 g) as an oil. 1H NMR (500 MHz, CDCl3): δ (ppm) 4.06-4.03 (m, 1H), 2.87 (s, 4H), 2.28-2.25 (m, 2H), 1.98-1.97 (m, 1H), 1.72-1.65 (m, 2H), 1.46-1.40 (m, 2H), 1.31-1.24 (m, 1H), 1.12-1.08 (m, 1H), 0.72-0.68 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328138B2
出典データセットuspto-grants-2016_05
ORD IDord-a462f20ee0eb40e099a1e0ec74193af1
出典メモuspto-grants-2016_05