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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235071생성일: 2026년 10월 25일

Potassium Carbonate → 5-Methyl-6-carboethoxy-7-amino-1H-pyrrolo[2,3-b]pyrazine

https://huagongshe.com/reaction/235071

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Ethyl N-methylaminoacetate hydrochlorideHCID 171173—
반응물3-Chloropyrazine-2-carbonitrileHCID 292465—
용매DimethylformamideHCID 6228—
생성물5-Methyl-6-carboethoxy-7-amino-1H-pyrrolo[2,3-b]pyrazineHCID 7028679831.1%

반응 단계

2-Chloro-3-cyanopyrazine (0.808 g, 5.79 mmol), prepared by the method of Shneller, et. al., J. Het. Chem., 12:513 (1975), was dissolved in 30 ml DMF under nitrogen and treated with sarcosine ethyl ester hydrochloride (0.978 g, 6.37 mmol) followed by K2CO3 (1.68 g, 12.16 mmol) at rt. The reaction mixture was gently refluxed for 36 h after which the cooled solution was partitioned between water and CHCl3. The aqueous phase was extracted with CHCl3 and the combined organics washed with water then brine and dried over Na2SO4. Concentration gave a green-black oil that was purified by chromatography on silica gel eluting with a gradient from 3:1 to 1:1 hexanes:ethyl acetate to give 0.40 g (31%) of the title compound as an orange solid. mp: 119°-121° C. 1H NMR (300 MHz, CDCl3) δ1.47 (t, 3H), 4.01 (s, 3H), 4.46 (q, 2H), 5.65 (br s, 2H), 8.32 (d, 1H), 8.38 (d, 1H). MS (DCI/NH3) m/e 220 (M+H)+. Analysis calc'd. for C10H12N4O2: C, 54.54; H, 5.49; N, 25.44; Found: C, 54.29; H, 5.52; N, 25.42.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05597823
출처 데이터셋uspto-grants-1997_01
ORD IDord-b18925ec9ba347d5ba4ee2e741c06ddf
출처 메모uspto-grants-1997_01