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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25165생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/25165

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물D-Tartaric acidHCID 439655—
반응물N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamideHCID 10247203—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
촉매HCID 178418397HCID 178418397—
생성물N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-cyanopyrrolo[1,2-a]pyrazine-3-carboxamide TartrateHCID 6977193347%

반응 조건

온도95 °C

반응 단계

To an argon sparged solution of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamide (0.77 g, 2.14 mmol) in DMF (25 mL) is added zinc cyanide (0.26 g, 2.20 mmol), and tetrakis(triphenylphosphine)palladium (0) (0.25 g, 0.21 mmol). The resulting suspension is stirred at 95° C. for 48 h, then filtered through a pad of celite. The residue is purified using preparative chromatography (carried out on a Chiral OD column using a 40% IPA/heptanes each containing 0.1% diethylamine) to give a pale yellow oil that is salted with d-tartaric acid and crystallized from EtOH/Et2O to give a pale yellow solid. Yield 47%. HRMS (FAB) calcd for C16H17N5O+H 296.1511, found 296.1520.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858613B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-35777fbdf51d4a96b2a0653b70a174ab
출처 메모uspto-grants-2005_02