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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 605906생성일: 2026년 10월 25일

Diisopropylethylamine → (5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-(3-fluoro-4-morpholin-4-yl-phenyl)-amine

https://huagongshe.com/reaction/605906

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3-Fluoro-4-morpholinoanilineHCID 1485330—
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)-(3-fluoro-4-morpholin-4-yl-phenyl)-amineHCID 5758999798.5%

반응 단계

This compound may be prepared using methods as described for Compound 6, step 1 using 5,8-dibromo-[1,2,4]triazolo[1,5-a]pyrazine (0.5 g, 1.799 mmol), 3-fluoro-4-morpholin-4-yl-phenylamine (0.53 g, 2.70 mmol), and DIPEA (0.470 mL, 2.70 mmol) in 2-propanol (6 mL). The reaction mixture is partitioned between 10% citric acid aqueous solution and DCM. The organic phase is separated and washed with water and brine, dried over MgSO4, filtered and concentrated under vacuum to afford the title compound (697 mg, 98%) which is used in the next step without further purification. LCMS: Rt 3.52 min (98.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915256B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-27112b23025d4d1797f595b435c6a5de
출처 메모uspto-grants-2011_03