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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618597Generated: November 3, 2026

6-Bromo-4-methoxy-1H-indole → 4-(6-bromo-4-methoxy-1H-indol-1-yl)-6-chloro-2,3-dimethylquinoline

https://huagongshe.com/reaction/1618597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-4-methoxy-1H-indoleHCID 24728034—
Reactant4,6-Dichloro-2,3-dimethylquinolineHCID 60994963—
Product4-(6-bromo-4-methoxy-1H-indol-1-yl)-6-chloro-2,3-dimethylquinolineHCID 67285059—

Reaction Steps

Prepared according to procedure U using 6-bromo-4-methoxy-1H-indole (0.05 g, 0.22 mmol) and 4,6-dichloro-2,3-dimethylquinoline (0.075 g, 0.33 mmol) to give 4-(6-bromo-4-methoxy-1H-indol-1-yl)-6-chloro-2,3-dimethylquinoline as a yellow solid: Mass Spectrum (ESI) m/e=415.0 [M+1 (79Br)] and 417.0 [M+1 (81Br)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765940B2
Source datasetuspto-grants-2014_07
ORD IDord-522b3c3d025c4aa98d56232c3b0cae1b
Source noteuspto-grants-2014_07