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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501542Generated: October 25, 2026

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

https://huagongshe.com/reaction/501542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(7R,7aS)-4-(7-Hydroxy-1,3-dioxotetrahydropyrrolo[1,2-c]imidazol-2-yl)-5,6,7,8-tetrahydronaphthalene-1-carbonitrileHCID 9904811—
ReactantN-(2,3-Dihydro-1H-inden-4-yl)acetamideHCID 12683814—
Reactant5-Nitroquinoline-8-carbonitrileHCID 21874838—
Reactant4-Isocyanato-5,6,7,8-tetrahydronaphthalene-1-carbonitrileHCID 59754304—
Product(7R,7aS)-5-(7-Hydroxy-1,3-dioxotetrahydropyrrolo[1,2-c]imidazol-2-yl)-quinoline-8-carbonitrileHCID 59754313—

Reaction Steps

The title compound was synthesized from compound 12C by procedures analogous to those described in Experiment 3A and Experiment 2 (2E to 2F). 99.8% at 2.05 min (retention time) (Conditions: YMC S5 ODS (4.6×50 mm); Eluted with 0% to 100% B; 4 min gradient; (A=90% H2O-10% MeOH-0.1% H3PO4 and B=10% H2O-90% MeOH-0.1% H3PO4); Flow rate at 4 mL/min. UV detection at 220 nm). LC/MS nm/z 309 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772267B2
Source datasetuspto-grants-2010_08
ORD IDord-361cbb36f79d4a8d8173a37d88efb6fb
Source noteuspto-grants-2010_08