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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243971생성일: 2026년 10월 25일

2-(Hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-quinoxaline → 2-{5-[(5-Fluoro-2-pyrimidin-2-ylphenyl)carbonyl]hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl}quinoxaline

https://huagongshe.com/reaction/243971

반응식

참여 물질

역할이름HCID투입량
반응물2-(Hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-quinoxalineHCID 61037281—
반응물5-Fluoro-2-(pyrimidin-2-yl)benzoic acidHCID 67086950—
생성물2-{5-[(5-Fluoro-2-pyrimidin-2-ylphenyl)carbonyl]hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl}quinoxalineHCID 67117215—

반응 단계

The title compound was prepared in a manner analogous to Example 15 utilizing Intermediate 35 and Intermediate 13. MS (ESI): mass calculated for C25H21FN6O, 440.48; m/z found 441.2 [M+H]+. 1H NMR (400 MHz, CDCl3): 8.71 (d, J=4.9, 2H), 8.37-8.30 (m, 2H), 7.92-7.88 (m, 1H), 7.72-7.69 (m, 1H), 7.63-7.57 (m, 1H), 7.43-7.37 (m, 1H), 7.23-7.17 (m, 1H), 7.11-7.05 (m, 2H), 4.03-3.93 (m, 2H), 3.87-3.70 (m, 3H), 3.67-3.56 (m, 2H), 3.26-3.03 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653263B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-902b2020a087442ebb0905b9595b06d5
출처 메모uspto-grants-2014_02