돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40670생성일: 2026년 10월 24일

5-Aminopyrazine-2-carbonitrile → 5-(1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridin-6-ylamino)pyrazine-2-carbonitrile

https://huagongshe.com/ko/reaction/40670

반응식

참여 물질

역할이름HCID투입량
반응물5-Aminopyrazine-2-carbonitrileHCID 13925294—
반응물Sodium t-butoxideHCID 23676156—
반응물1-(4-methoxybenzyl)-6-bromo-1H-imidazo[4,5-c]pyridineHCID 56926466—
촉매palladium(II) acetateHCID 167845—
용매Dimethylformamide tolueneHCID 21735183—
생성물5-(1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridin-6-ylamino)pyrazine-2-carbonitrileHCID 4420435740%

반응 조건

온도150 °C

반응 단계

Palladium (II) acetate (3.5 mg, 16 μmol) was added to (±)-2,2″-bis(diphenylphosphino)-1,1″-binaphthalene (59 mg, 94 μmol) in DMF/toluene (1:2) and the resulting mixture was degassed under a stream of nitrogen gas for 10 minutes. 2-Amino-5-cyanopyrazine (19 mg, 0.16 mmol), sodium tert-butoxide (45 mg, 0.47 mmol) and 1-(4-methoxybenzyl)-6-bromo-1H-imidazo[4,5-c]pyridine (50 mg, 0.16 mmol) were added and the mixture was degassed for a further 5 minutes before heating at 150° C. for 30 minutes using microwave irradiation. The reaction mixture was partitioned between water and dichloromethane. The aqueous phase extracted with dichloromethane. The combined organic layers were dried (Na2SO4) and concentrated. The residue was dissolved in methanol, passed through a PS-Thiol column and concentrated. The product was purified using preparative HPLC to give the title compound (22.4 mg, 40%). 1H NMR (d6-DMSO, 400 MHz) δ 10.84 (br s, 1H), 8.77 (d, 1H, J=1.3 Hz), 8.74 (m, 2H), 8.49 (s, 1H), 8.17 (s, 1H), 7.34 (m, 2H), 5.41 (s, 2H), 3.72 (s, 3H). LCMS (2) Rt=2.32 min; m/z (ESI+) 358 (MH+), (ESI−) 356 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530468B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-68a88dca70fb4c9daa1ea5cb4026c9b2
출처 메모uspto-grants-2013_09