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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067262Generated: October 30, 2026

Propargyl alcohol → HCID 16073857, compound

https://huagongshe.com/reaction/1067262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantHCID 21192417HCID 21192417—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
ProductHCID 16073857HCID 16073857—

Reaction Steps

To a stirred slurry of 1.15 g of 1-(tert-butyl)-N-(4-chlorobenzyl)-6-iodo-4-oxo-1,4-dihydro-3-quinolinecarboxamide from Preparation No. 10, 156 mg of copper (I) iodide, and 66 mg of dichlorobis(triphenylphosphine)palladium (II) in 23 mL of diethylamine, under argon, is added 0.16 mL of propargyl alcohol. The mixture is stirred for 18 hour at room temperature, then concentrated under reduced pressure. The residue is partitioned between water and chloroform-methanol, and the organic phase dried (MgSO4) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 2-4% methanol in dichloromethane affords 977 mg of tan solid. Recrystallization from ethanol provides 850 mg of the title compound as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248736B1
Source datasetuspto-grants-2001_06
ORD IDord-da0514078bbf4c3e9a12cf593bc085db
Source noteuspto-grants-2001_06