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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69592생성일: 2026년 10월 25일

Diisopropylethylamine → (S)-N-ethyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide

https://huagongshe.com/reaction/69592

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(Cyanomethyl)trimethylphosphanium iodideHCID 10514344—
반응물N-ethyl-4-(piperazin-1-yl)benzamideHCID 28749590—
반응물(S)-3-(hydroxymethyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-oneHCID 58324378—
용매Dimethyl SulfoxideHCID 679—
용매PropionitrileHCID 7854—
생성물(S)-N-ethyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamideHCID 46864826—

반응 조건

온도90 °C

반응 단계

To a suspension of (S)-3-(hydroxymethyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one (0.8 g, 3.65 mmol)) in propiononitrile (Volume: 27.4 ml) was added (cyanomethyl)trimethylphosphonium iodide (1.064 g, 4.38 mmol), N-ethyl-4-(piperazin-1-yl)benzamide (0.851 g, 3.65 mmol) and DIEA (1.912 ml, 10.95 mmol). The vial was heated to 90° C. for 16 hours. The crude reaction was cooled to RT, DMSO (1 ml) was added, and the mixture was purified via HPLC (55-90, basic) to give the product as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822470B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9fc43a7fa9e6457ca5488b23c8f0c36f
출처 메모uspto-grants-2014_09