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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828718Generated: November 2, 2026

Benzoyl chloride, 3,4-dichloro- → HCID 22057976, compound

https://huagongshe.com/reaction/1828718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantHCID 22057974HCID 22057974—
SolventTriethylamineHCID 8471—
ProductHCID 22057976HCID 2205797657%

Reaction Steps

Using an analogous procedure to that described in Example 4, 3,4-dichlorobenzoyl chloride was reacted with N-(5-amino-2-methylphenyl)quinoline-6-carboxamide in the presence of triethylamine. The reaction mixture was stirred at ambient temperature for 16 hours and then evaporated. The residue was purified by column chromatography on silica using increasingly polar mixtures of methylene chloride and methanol as eluent. There was thus obtained the title compound in 57% yield; Mass Spectrum: M+H+ 450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060700B2
Source datasetuspto-grants-2006_06
ORD IDord-7711a4b58b77402fa9925ea9c6d141c9
Source noteuspto-grants-2006_06