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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 543546생성일: 2026년 10월 26일

Sodium hydride → 5-[(2,6-dimethoxyphenyl)methyl]-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one

https://huagongshe.com/reaction/543546

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-oneHCID 2766187—
반응물2-(chloromethyl)-1,3-dimethoxyBenzeneHCID 12707002—
반응물HCID 178418361HCID 178418361—
용매DimethylformamideHCID 6228—
생성물5-[(2,6-dimethoxyphenyl)methyl]-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-oneHCID 1334208089%

반응 단계

To a stirred solution of 6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one (2.7 g. 0.01 mole) in 30 ml. of dry dimethyl formamide was added sodium hydride (0.5 g., 0.02 mole of 50% dispersion in mineral oil). When the evolution of hydrogen subsides, 2.7 g. (0.01 mole) of 2,6-dimethoxybenzyl chloride was added. The reaction mixture was stirred at room temperature for eighteen hours, and the dimethyl formamide was removed under vacuo. The residue was triturated with cold water, filtered and recrystallized from ethanol to give white crystals of the title compound, 2.7 g. (89% yield) m.p. 200°-202° C.; hydrochloride salt, m.p. 220°-223° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04446323
출처 데이터셋uspto-grants-1984_05
ORD IDord-6583a93d32e343f8b31f9da4155b9909
출처 메모uspto-grants-1984_05