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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784098Generated: October 29, 2026

2-Bromoethanol → 7-(2-Bromoethoxy)-3-cyano-6-methoxy-4-(2,3-methylenedioxyanilino)quinoline

https://huagongshe.com/reaction/1784098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
Reactant3-Cyano-7-hydroxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinolineHCID 135494159—
Product7-(2-Bromoethoxy)-3-cyano-6-methoxy-4-(2,3-methylenedioxyanilino)quinolineHCID 1798051382%

Reaction Steps

Using an analogous procedure to that described in Example 8, 3-cyano-7-hydroxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinoline was reacted with 2-bromoethanol to give the title compound in 82% yield; NMR Spectrum: (DMSOd6) 3.88 (t, 2H), 3.94 (s, 3H), 4.51 (t, 2H), 5.96 (s, 2H), 6.8-6.93 (m, 3H), 7.34 (s, 1H), 7.8 (s, 1H), 8.42 (s, 1), 9.53 (s, 1H); Mass Spectrum: M+H+ 444.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501516B2
Source datasetuspto-grants-2009_03
ORD IDord-cd01101c1137484d92df54c3e56ba1c6
Source noteuspto-grants-2009_03