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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11045생성일: 2026년 10월 24일

Pyridinium hydrochloride → 4-(3,5-Dinitrophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione

https://huagongshe.com/ko/reaction/11045

반응식

참여 물질

역할이름HCID투입량
반응물Pyridinium hydrochlorideHCID 21584435—
반응물4-(3,5-dinitrophenyl)-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dioneHCID 86760191—
생성물4-(3,5-Dinitrophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dioneHCID 8676019257%

반응 단계

The reaction of 4-(3,5-dinitrophenyl)-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione (V; Ar=3,5-dinitrophenyl, R10═H) (42) prepared as described in example 48 with pyridinium hydrochloride according to the proceedure described in example 81 gave 4-(3,5-Dinitrophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione (V; Ar=3,5-dinitrophenyl, R10═H) (43) in a 57% yield as an orange powder, mp>330° C. 1H NMR δ [(CD3)2SO] 11.94 (br s, 1H), 11.18 (br s, 1H), 9.32 (br s, 1H), 8.91 (s, 3H), 8.35 (d, J=2.3 Hz, 1H), 7.83 (s, 1H), 7.49 (d, J=8.7 Hz, 1H), 7.11 (dd, J=8.7, 2.3 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094798B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-9646ed85d1e945ff98b8b534569f0755
출처 메모uspto-grants-2006_08