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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50164Generated: October 27, 2026

6-Bromo4-(3-ethoxy-phenyl)-2-methoxy-quinoline → (5-chloro-thiophen-2-yl)-[4-(3-ethoxy-phenyl)-2-methoxy-quinolin-6-yl]-(3-methyl-3H-imidazol-4-yl)-methanol

https://huagongshe.com/reaction/50164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo4-(3-ethoxy-phenyl)-2-methoxy-quinolineHCID 22465419—
Reactant(5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanoneHCID 22465441—
Product(5-chloro-thiophen-2-yl)-[4-(3-ethoxy-phenyl)-2-methoxy-quinolin-6-yl]-(3-methyl-3H-imidazol-4-yl)-methanolHCID 2246541872%

Reaction Steps

Following the same procedure as that described in example 1E, 6-bromo-4-(3-ethoxy-phenyl)-2-methoxy-quinoline (800 mg, 2.23 mmol) and (5chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanone (610 mg, 2.68 mmol) generated the title compound of 23B (810 mg, 72% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710209B2
Source datasetuspto-grants-2004_03
ORD IDord-9b3bcb06ca1644a9a27ccf01fbe8c254
Source noteuspto-grants-2004_03