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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25164생성일: 2026년 10월 25일

Propargyl alcohol → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-(3-hydroxyprop-1-ynyl)pyrrolo[1,2-a]pyrazine-3-carboxamide tartrate

https://huagongshe.com/reaction/25164

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참여 물질

역할이름HCID투입량
반응물Propargyl alcoholHCID 7859—
반응물TriethylamineHCID 8471—
반응물D-Tartaric acidHCID 439655—
반응물N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromopyrrolo[1,2-a]pyrazine-3-carboxamideHCID 10247203—
촉매HCID 178418903HCID 178418903—
촉매HCID 178505377HCID 178505377—
용매1,4-DioxaneHCID 31275—
생성물N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-(3-hydroxyprop-1-ynyl)pyrrolo[1,2-a]pyrazine-3-carboxamide tartrateHCID 6977234424%

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온도80 °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 (0.230 g, 0.92 mmol), triethylamine (3.2 mL, 23.0 mmol) in dioxane (5 mL) is added copper (I) iodine (0.054 g, 0.28 mmol), propargyl alcohol (0.22 mL, 3.68 mmol), and dichlorobis(triphenylphosphino)-palladium (II) (0.063 g, 0.09 mmol). The reaction vessel is purged with argon, and stirred at 80° C. for 20 h at which point it is filtered through a plug of celite, concentrated to dryness, and the residue dissolved in CHCl3 (150 mL) that is washed with a solution containing 1:1 NH4OH/brine (5×35 mL). The residue is purified using silica gel chromatography (5% MeOH/CH2Cl2 gradient up to 10% MeOH/CH2Cl2) to give a pale orange colored oil that is salted with d-tartaric acid, and crystallized from EtOH/Et2O to give a tan solid. Yield 24%. HRMS (FAB) calcd for C18H20N4O2+H 325.1664, found 325.1664.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858613B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-0ee1fb5b7808414d8920f6aced541af2
출처 메모uspto-grants-2005_02