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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925952Generated: October 29, 2026

2,8-Dichloro-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline → 2-Chloro-6-methoxy-4-(4-methoxybenzyloxy)-8-methyl-quinoline

https://huagongshe.com/reaction/925952

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,8-Dichloro-7-methoxy-4-(4-methoxy-benzyloxy)-quinolineHCID 56605153—
Reactant2,4-Dichloro-6-methoxy-8-methyl-quinolineHCID 86627750—
Product2-Chloro-6-methoxy-4-(4-methoxybenzyloxy)-8-methyl-quinolineHCID 8662775158%

Reaction Steps

2-Chloro-6-methoxy-4-(4-methoxybenzyloxy)-8-methyl-quinoline 221f was synthesized from compound 220f as a white solid in 58% yield, following the procedure as described for compound 221d. 1H NMR (CDCl3, 400 MHz) δ (ppm) 2.68 (s, 3H), 3.80 (s, 3H), 3.83 (s, 3H), 5.11 (s, 2H), 6.72 (s, 1H), 6.97 (d, J=9.03 Hz, 2H), 7.15 (dd, J=3.01 Hz and J=0.96 Hz, 1H), 7.20 (d, J=3.00 Hz, 1H), 7.40 (d, J=9.03 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284307B2
Source datasetuspto-grants-2016_03
ORD IDord-345665ecc2214309bd7754378f8b0241
Source noteuspto-grants-2016_03