돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1908985생성일: 2026년 10월 24일

Pyrazole → 2-Bromo-6-(1H-pyrazol-1-yl)pyridine

https://huagongshe.com/ko/reaction/1908985

반응식

참여 물질

역할이름HCID투입량
반응물PyrazoleHCID 1048—
반응물2,6-DibromopyridineHCID 12274—
반응물Potassium tert-butoxideHCID 23665647—
용매1,4-DioxaneHCID 31275—
생성물2-Bromo-6-(1H-pyrazol-1-yl)pyridineHCID 706052990%

반응 단계

To a solution of 1H-Pyrazole (10.0 mmol, 680 mg) in distilled dioxane (30 mL) were added KOtBu (11.0 mmol, 1.26 g), and followed by addition of 2,6-dibromopyridine (10.0 mmol, 2.37 g). The reaction mixture was refluxed for 48 hour, and then quenched with 5 mL of water. Solvent was removed under reduced pressure and water was added to the residue, then the mixture was extracted with DCM. The combined organic layers were washed with brine and dried over MgSO4. After solvent evaporation, the crude product was purified by column chromatography on silica gel (Hexanes:ethyl acetate=20:1 as eluent) to afford a white solid (2.01 g, 90%). 1H NMR (400 MHz, CDCl3, ppm): 8.53 (s, 1H), 7.92 (d, 1H, J=7.6 Hz), 7.73 (s, 1H), 7.67 (t, 1H, J=7.8 Hz), 7.35 (d, 1H, 7.6 Hz), 6.46 (s, 1H). 13C NMR (100 MHz, CDCl3, ppm): 162.72, 140.73, 139.91, 127.58, 125.25, 110.89, 108.23.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598351B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-95e63f97ec00497b9e4dd19c82b313a5
출처 메모uspto-grants-2013_12