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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217772생성일: 2026년 10월 24일

Sodium Carbonate → 3-Amino-6-(4-(3-(tert-butyldimethylsilyloxy)propyl)phenyl)-N-(pyridin-3-yl)-pyrazine-2-carboxamide

https://huagongshe.com/ko/reaction/217772

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Potassium AcetateHCID 517044—
반응물Bis(pinacolato)diboraneHCID 2733548—
반응물3-Amino-6-bromo-N-pyridin-3-ylpyrazine-2-carboxamideHCID 10402162—
반응물HCID 15342962HCID 15342962—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물3-Amino-6-(4-(3-(tert-butyldimethylsilyloxy)propyl)phenyl)-N-(pyridin-3-yl)-pyrazine-2-carboxamideHCID 6667865062.3%

반응 단계

A mixture of the product of step (ii) (9.84 g, 30 mmol), bis(pinacolato)diboron (11.4 g, 45 mmol), KOAc (9 g, 90 mmol) and Pd(dppf)Cl2 (1 g, 1.5 mmol) in dioxane (200 mL) was stirred and degassed with N2 (×3). The mixture was stirred at 80° C. under a N2 atmosphere for 3 hours. The reaction mixture was cooled to room temperature. Water (25 mL) and Na2CO3 (10 g, 90 mmol) were added to the mixture. The mixture was stirred for 10 minutes before the product of step (v) (7.9 g, 27 mmol) and Pd(dppf)Cl2 (0.5 g, 0.7 mmol) were added. The resulting solution was degassed again with N2 (×3). The reaction mixture was stirred at 90° C. under a N2 atmosphere for additional 10 hours. Na2SO4 was added, filtered and the filtrate concentrated in vacuo. The crude product was purified by column chromatography with PE:EtOAc=5:1 to 3:1 as eluent to afford the subtitle compound (vi) as a yellow solid (7.8 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198285B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-8f06ac597e2842a492e02395d14ac654
출처 메모uspto-grants-2012_06