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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241413생성일: 2026년 10월 24일

Sodium Carbonate → 3-(1H-imidazo[4,5-b]pyridin-2-yl)-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamine

https://huagongshe.com/ko/reaction/241413

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
반응물5-bromo-3-(1H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-ylamineHCID 66869810—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물3-(1H-imidazo[4,5-b]pyridin-2-yl)-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamineHCID 66898551—

반응 단계

58 mg (0.200 mmol) of 5-bromo-3-(1H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-ylamine and 45.8 mg (0.220 mmol) of 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole are suspended in 2 ml of N,N-dimethylformamide in a nitrogen-filled microwave vessel, and 0.57 ml (1.142 mmol) of 2M sodium carbonate solution and 23.1 mg (0.020 mmol) of tetrakis(triphenylphosphine)palladium(0) are added. The reaction solution is irradiated with microwaves for 30 min at 120° C. in the Biotage SmithSynthesizer. The reaction mixture is evaporated to dryness, and the residue is purified by means of RP-HPLC, giving 3-(1H-imidazo[4,5-b]pyridin-2-yl)-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamine; HPLC-MS [M+H]+ 292.2;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648201B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-a1ef29d4a7fb4ec281e9f0fd034bb37c
출처 메모uspto-grants-2014_02