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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41540생성일: 2026년 10월 23일

Dimethylformamide → 2-(Naphthalen-1-ylmethyl)-9-(quinoxalin-2-yl)-2,9-diazaspiro[5.5]undecan-1-one

https://huagongshe.com/ko/reaction/41540

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물1-ChloromethylnaphthaleneHCID 6845—
반응물Sodium hydrideHCID 24758—
반응물tert-Butyl 1-oxo-2,9-diazaspiro[5.5]undecane-9-carboxylateHCID 49760149—
촉매Tetrabutylammonium IodideHCID 67553—
용매TetrahydrofuranHCID 8028—
생성물2-(Naphthalen-1-ylmethyl)-9-(quinoxalin-2-yl)-2,9-diazaspiro[5.5]undecan-1-oneHCID 5325911161%

반응 단계

A solution of tert-butyl 1-Oxo-2,9-diaza-spiro[5.5]undecane-9-carboxylate (400 mg, 1.5 mmol) in DMF (2 ml) was added slowly at rt to a suspension of sodium hydride 95% (54 mg, 2.24 mmol) in THF (6 ml). The reaction mixture was stirred for 20 min at rt. Then a solution of 1-(chloromethyl)naphthalene (0.33 ml, 2.24 mmol) in THF (2 ml) was added dropwise followed by the addition of tetrabutylammonium iodide (55 mg, 0.15 mmol). The mixture was stirred at 45° C. for 18 h. The reaction mixture was quenched with H2O (50 ml) and extracted twice with EtOAc (50 ml). The combined organic layer was dried over Na2SO4, filtered and evaporated. The residue was purified by flash chromatography (hexane/EtOAc 2:1) to yield 377 mg (61%) of the title compound. [1H NMR (DMSO, 400 MHz) δ 8.01 (m, 1H), 7.93 (m, 1H), 7.85 (m, 1H), 7.55-7.42 (m, 3H), 7.30 (m, 1H), 4.95 (s, 2H), 3.72 (m, 2H), 3.15-2.95 (m, 4H), 1.98-1.82 (m, 2H), 1.78-1.62 (m, 4H), 1.48-1.38 (m, 2H), 1.39 (s, 9H)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530648B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-393facae0d6c422b8d21b173d5c6f557
출처 메모uspto-grants-2013_09