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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501545생성일: 2026년 10월 24일

(7R,7aS)-4-(7-Hydroxy-1,3-dioxotetrahydropyrrolo[1,2-c]imidazol-2-yl)-5,6,7,8-tetrahydronaphthalene-1-carbonitrile → (7R,7aS)-4-(7-Hydroxy-1,3-dioxotetrahydropyrrolo[1,2-c]imidazol-2-yl)isoquinoline-1-carbonitrile

https://huagongshe.com/ko/reaction/501545

반응식

참여 물질

역할이름HCID투입량
반응물(7R,7aS)-4-(7-Hydroxy-1,3-dioxotetrahydropyrrolo[1,2-c]imidazol-2-yl)-5,6,7,8-tetrahydronaphthalene-1-carbonitrileHCID 9904811—
반응물4-Aminoisoquinoline-1-carbonitrileHCID 21875272—
반응물4-Isocyanato-5,6,7,8-tetrahydronaphthalene-1-carbonitrileHCID 59754304—
생성물(7R,7aS)-4-(7-Hydroxy-1,3-dioxotetrahydropyrrolo[1,2-c]imidazol-2-yl)isoquinoline-1-carbonitrileHCID 59754226—

반응 단계

The title compound was synthesized from compound 13D by procedures analogous to those described in Experiment 2E to 2F. HPLC: 97.6% at 1.54 min (retention time) (Conditions: YMC S5 C-18 (4.6×50 mm); Eluted with 0% to 100% B; 4 min gradient; (A=90% H2O-10% MeCN-0.1% TFA and B=10% H2O-90% MeCN-0.1% TFA); Flow rate at 4 mL/min. UV detection at 220 nm). LC/MS m/z 309 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772267B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-26ca626ac4304e34854a1eb9e9fd1212
출처 메모uspto-grants-2010_08