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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72122생성일: 2026년 10월 25일

1-Propanol → (R)-tert-butyl 3-(5-cyanopyridin-2-ylamino)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/72122

반응식

참여 물질

역할이름HCID투입량
반응물1-PropanolHCID 1031—
반응물DiisopropylethylamineHCID 81531—
반응물(R)-(+)-1-Boc-3-aminopyrrolidineHCID 854070—
반응물2-Fluoropyridine-5-carbonitrileHCID 15765964—
용매Ethyl AcetateHCID 8857—
생성물(R)-tert-butyl 3-(5-cyanopyridin-2-ylamino)pyrrolidine-1-carboxylateHCID 6688494489.6%

반응 조건

온도150 °C

반응 단계

A heavy-walled, screw-cap glass tube was charged with (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate (3.30 g, 17.7 mmol), 2-fluoro-5-cyanopyridine (1.63 g, 13.2 mmol), i-Pr2NEt (6.3 mL, 35.5 mmol) and n-PrOH (3 mL). The mixture was heated at 150° C. in an oil bath for 2 h. The mixture was diluted with EtOAc (180 mL), washed with 1% aq HCl (3×40 mL), satd aq NaHCO3 (40 mL) and brine (40 mL), and dried over Na2SO4. Removal of the solvent left an oil (3.28 g) which was purified by chromatography on a 40-g silica gel cartridge eluted with a 0-100% EtOAc in hexanes gradient to afford (R)-tert-butyl 3-(5-cyanopyridin-2-ylamino)pyrrolidine-1-carboxylate (3.41 g, 88% based on 2-fluoro-5-cyanopyridine). LC-MS Method 1 tR=1.57 min, m/z=289.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828985B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-7ee7d64f5f4e4e9aa1ddbbf045262891
출처 메모uspto-grants-2014_09