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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25162생성일: 2026년 10월 25일

Diisopropylethylamine → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamide

https://huagongshe.com/reaction/25162

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Tetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물6-Bromopyrrolo(1,2-a)pyrazine-3-carboxylic acid hydrochlorideHCID 69713212—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamideHCID 10247203—

반응 단계

To a suspension of 6-bromopyrrolo[1,2-a]pyrazine-3-carboxylic acid hydrochloride (1.67 mmol), (R)-3-aminoquinulidine dihydrochloride (0.34 g, 1.67 mmol), DIEA (1.5 mL, 8.35 mmol) in DMF (20 mL) and THF (10 mL) is added HATU (0.64 g, 1.67 mmol). The resulting suspension is stirred for 16 h at which time it is concentrated to dryness under reduced pressure. The resulting material is absorbed to silica gel and purified with silica gel chromatography (9% MeOH/1%NH3OH/CH2Cl2 as the eluent) salted with fumeric acid, and crystallized from EtOH/acetone/Et2O to give an off white spheres. Yield 45%. HRMS (FAB) calcd. for C15H17BrN4O+H 349.0664, found 349.0647.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858613B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-719641f08ec94b06a39361fb8608fa61
출처 메모uspto-grants-2005_02