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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880767Generated: October 31, 2026

2,4-Dichloro-7-methoxy-8-methylquinoline → 2-Chloro-8-methyl-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline

https://huagongshe.com/reaction/880767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-7-methoxy-8-methylquinolineHCID 53400954—
Reactant2,8-Dichloro-7-methoxy-4-(4-methoxy-benzyloxy)-quinolineHCID 56605153—
Product2-Chloro-8-methyl-7-methoxy-4-(4-methoxy-benzyloxy)-quinolineHCID 5660515950%

Reaction Steps

2-Chloro-8-methyl-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline 221b was synthesized from compound 220b as a white powder in 50% yield, following the procedure as described for compound 221d. 1H NMR (CDCl3, 376 MHz) δ (ppm) 2.60 (s, 3H), 3.85 (s, 3H), 3.97 (s, 3H), 5.18 (s, 2H), 6.69 (s, 1H), 6.97 (d, J=8.57 Hz, 1H), 7.19 (d, J=8.57 Hz, 1H), 7.42 (d, J=8.57 Hz, 1H), 8.02 (d, J=8.57 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993595B2
Source datasetuspto-grants-2015_03
ORD IDord-c482e62be7164fa59d1fa6ce74c0bbd1
Source noteuspto-grants-2015_03