돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 522361생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/522361

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Di(succinimido) carbonateHCID 676246—
반응물rel-(1R,2R)-2-(pent-4-en-1-yl)cyclopropan-1-olHCID 67304189—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매Diethyl EtherHCID 3283—
용매AcetonitrileHCID 6342—
생성물1-[({[(1R,2R)-2-(pent-4-yn-1-yl)cyclopropyl]oxy}carbonyl)oxy]pyrrolidine-2,5-dioneHCID 89590835—

반응 조건

온도40 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328138B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-a462f20ee0eb40e099a1e0ec74193af1
출처 메모uspto-grants-2016_05