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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 5-Aminopyrazine-2-carbonitrile | HCID 13925294 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 반응물 | 1-(4-methoxybenzyl)-6-bromo-1H-imidazo[4,5-c]pyridine | HCID 56926466 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Dimethylformamide toluene | HCID 21735183 | — |
| 생성물 | 5-(1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridin-6-ylamino)pyrazine-2-carbonitrile | HCID 44204357 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08530468B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-68a88dca70fb4c9daa1ea5cb4026c9b2 |
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| 출처 메모 | uspto-grants-2013_09 |
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