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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384346Generated: October 31, 2026

6-Bromo-4-(3-chlorophenyl)-2-methoxyquinoline → [4-(3-chloro-phenyl)-2-methoxy-quinolin-6-yl]-(5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanol

https://huagongshe.com/reaction/1384346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-4-(3-chlorophenyl)-2-methoxyquinolineHCID 12016672—
Reactant(5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanoneHCID 22465441—
Product[4-(3-chloro-phenyl)-2-methoxy-quinolin-6-yl]-(5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanolHCID 2246541199%

Reaction Steps

Following the same procedure as described in example 1E, 6-bromo-4-(3-chloro-phenyl)-2-methoxy-quinoline (1.0 g, 1.87 mmol) and (5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanone (170 mg, 3.44 mmol) generated the title compound of 18A as a yellow solid (919 mg, 65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258824B1
Source datasetuspto-grants-2001_07
ORD IDord-7b6f638c8f10422b8c3fdd2f75a7c0c0
Source noteuspto-grants-2001_07