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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45153생성일: 2026년 10월 23일

2,2'-Bipyridine → 1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole

https://huagongshe.com/ko/reaction/45153

반응식

참여 물질

역할이름HCID투입량
반응물2,2'-BipyridineHCID 1474—
반응물Sodium CarbonateHCID 10340—
반응물5-Cyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazoleHCID 59394660—
촉매Cupric acetateHCID 8895—
용매1,2-DichloroethaneHCID 11—
생성물1,5-Dicyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazoleHCID 59394790104.2%

반응 조건

온도70 °C

반응 단계

A suspension of copper (II) acetate (0.902 g, 4.97 mmol) and 2,2′-bipyridine (0.776 g, 4.97 mmol) in DCE (20 mL) is stirred at 70° C. for 15 min, then transferred to a suspension of cyclopropyl trifluoroborate potassium salt (1.47 g, 9.94 mmol) and 5-Cyclopropyl-3-(2,5-dimethyl-pyrrol-1-yl)-1H-pyrazole (1 g, 4.97 mmol), and sodium carbonate (1.053 g, 9.94 mmol) in DCE (40 mL). The resulting dark-green mixture is stirred at 70° C. for 24 h. T The reaction mixture is partitioned between EtOAc and 1N HCl. The aqueous layer is extracted with EtOAc. The combined organic layers are washed with brine, dried (Na2SO4) and concentrated. The residue (1.64 g) is purified by ISCO (EtOAc-heptane 0-30%) to provide the desired product (1.25 g) as a colorless oil. MS (ESI) m/z 242.3 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541432B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d2d5fd8e56d141a08b39d578e86e99af
출처 메모uspto-grants-2013_09