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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827263Generated: October 27, 2026

2-Furancarbonyl chloride → (+/-)-N-[4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(1-methyl-1H-imidazol-5-yl)methyl]-2-quinolinyl]-2-furancarboxamide

https://huagongshe.com/reaction/1827263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarbonyl chlorideHCID 68242—
Reactant(+/-)-2-amino-4-(3-chlorophenyl)-alpha-(4-chlorophenyl)-alpha-(1-methyl-1H-imidazol-5-yl)-6-quinolinemethanolHCID 12083367—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-N-[4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(1-methyl-1H-imidazol-5-yl)methyl]-2-quinolinyl]-2-furancarboxamideHCID 22136488—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of (±)-2-amino-4-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(1-methyl-1H-imidazol-5-yl)-6-quinolinemethanol (0.00021 mol), described in International Patent Specification WO 00/39082, and 2-furancarbonyl chloride (0.00063 mol) in THF (1 ml) was heated for 5 hours at 60° C. The solvent was evaporated and the residue was purified by HPLC. The product fractions were collected and the solvent was evaporated, yielding (±)-N-[4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(1-methyl-1H-imidazol-5-yl)methyl]-2-quinolinyl]-2-furancarboxamide, MS (ESI) m/z: 569 571 573.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053105B2
Source datasetuspto-grants-2006_05
ORD IDord-91bd9c6890aa47eaaa6770a19afb2834
Source noteuspto-grants-2006_05