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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1783956생성일: 2026년 10월 25일

Diisopropylethylamine → (5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-amine

https://huagongshe.com/reaction/1783956

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-(2-Morpholinoethoxy)anilineHCID 6484711—
반응물5,8-Dibromo-(1,2,4)triazolo(1,5-a)pyrazineHCID 49758022—
반응물4-{8-[4-(4-Methyl-piperazin-1-yl)-phenylamino]-[1,2,4]triazolo[1,5-a]pyrazin-5-yl}-thiophene-2-carboxylic acid amideHCID 57589928—
용매IsopropanolHCID 3776—
생성물(5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-amineHCID 5759005286.2%

반응 조건

온도95 °C

반응 단계

According to the procedure described for Compound 6, step 1, 5,8-dibromo-[1,2,4]triazolo[1,5-a]pyrazine (0.5 g, 1.799 mmol), 4-(2-morpholin-4-yl-ethoxy)-phenylamine (0.6 g, 4.5 mmol) and N,N-diisopropylethylamine (0.47 mL, 2.7 mmol) in 2-propanol (6 mL) are stirred at 95° C. overnight. After evaporation of the solvent the residue is dissolved in DCM and washed with water (2×) and brine. The organic layer is dried over MgSO4, filtered and concentrated in vacuo to afford an oil purified by silica gel column chromatography. Elution with a 97:3 mixture DCM:MeOH gives the title compound (650 mg 86%) as a light yellow solid. LCMS: Rt 2.06 nm in (97.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07501411B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-c81a802209604c4eadda7d37f101c2c4
출처 메모uspto-grants-2009_03