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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78564생성일: 2026년 10월 24일

Sodium Carbonate → 3-Amino-6-(pyridin-3-yl)pyrazine-2-carboxylic acid

https://huagongshe.com/ko/reaction/78564

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물TriphenylphosphineHCID 11776—
반응물Methyl 3-Amino-6-bromopyrazine-2-carboxylateHCID 227251—
반응물3-(Diethylboryl)pyridineHCID 642851—
촉매Palladium ChlorideHCID 24290—
용매1,2-DimethoxyethaneHCID 8071—
용매Ethyl AcetateHCID 8857—
생성물3-Amino-6-(pyridin-3-yl)pyrazine-2-carboxylic acidHCID 5947215483.4%

반응 단계

A mixture of methyl 3-amino-6-bromo-pyrazine-2-carboxylate (8 g, 34.48 mmol), diethyl-(3-pyridyl)borane (6.084 g, 41.38 mmol), dichloropalladium; triphenylphosphane (1.210 g, 1.724 mmol) and disodium carbonate (51.70 mL of 2 M, 103.4 mmol) in DME (100 mL) were heated overnight at 80° C. The reaction mixture was cooled and EtOAc was added. The resultant precipitate was collected, treated with water and the resultant suspension heated and filtered hot. The solution was then allowed to cool and acidified with AcOH to approx pH 5. The precipitate was collected, washed with MeOH and dried to yield the product as a yellow powder (6.22 g, 83% Yield). 1H NMR (400.0 MHz, DMSO) d 7.49 (dd, J=4.8, 7.4 Hz, 1H), 7.60 (s, 2H), 8.44 (d, J=7.6 Hz, 1H), 8.57 (d, J=3.7 Hz, 1H), 8.97 (s, 1H) and 9.27 (s, 1H) ppm; MS (ES+) 217

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841308B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-90c9a609f1164fa2800eafbbc9caf6e9
출처 메모uspto-grants-2014_09