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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454881생성일: 2026년 10월 25일

tert-butyl 4-(3-((1-(quinolin-2-yl)azetidin-3-yl)oxy)pyrazin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(3-((1-(quinolin-2-yl)azetidin-3-yl)oxy)pyrazin-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/454881

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl 4-(3-((1-(quinolin-2-yl)azetidin-3-yl)oxy)pyrazin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 58547770—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물Tert-butyl 4-(3-((1-(quinolin-2-yl)azetidin-3-yl)oxy)pyrazin-2-yl)piperidine-1-carboxylateHCID 5854812986%

반응 단계

A mixture of tert-butyl 4-(3-((1-(quinolin-2-yl)azetidin-3-yl)oxy)pyrazin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (459 mg, 1.0 mmol) and wet Pd—C (50%, 300 mg) in MeOH (20 mL) was stirred under H2 (30 psi) at room temperature overnight then the reaction mixture was filtered through and washed with MeOH. The filtrate was concentrated in vacuo to give tert-butyl 4-(3-((1-(quinolin-2-yl)azetidin-3-yl)oxy)pyrazin-2-yl)piperidine-1-carboxylate (400 mg, 0.86 mmol, yield 86%). ESI-MS (M+1): 463 calc. for C26H31N5O3 462.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497265B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-0de6415f186e4d5cb889264940e7bf3d
출처 메모uspto-grants-2013_07