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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841540Generated: November 3, 2026

3-Butyn-1-OL → HCID 491972, compound

https://huagongshe.com/reaction/1841540

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Butyn-1-OLHCID 13566—
ReactantHCID 178522927HCID 178522927—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
ProductHCID 491972HCID 49197271%

Reaction Steps

A solution of N-(4-chlorobenzyl)-4-hydroxy-8-iodo-6-(tetrahydro-2H-pyran-4-ylmethyl)-3-quinolinecarboxamide (0.16 g), PdCl2(PPh3)2, CuI (0.018 g) and 3-butyn-1-ol (0.03 mL) in 15 mL Et2NH is stirred at room temperature for 7 days. The solid in the reaction is filtered and rinsed with EtOAc. The filtrate is partitioned between EtOAc and H2O. The aqueous layer is extracted with EtOAc (3×). The organic layers and the solid previously filtered are combined, concentrated, adsorbed onto silica and chromatographed (gradient from CH2Cl2 to 4% MeOH in CH2Cl2). Product-containing fractions are combined and condensed to afford 101.6 mg (71%) of N-(4-chlorobenzyl)-2-(2-hydroxyethyl)-6-oxo-8-(tetrahydro-2H-pyran-4-ylmethyl)-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxamide as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683181B2
Source datasetuspto-grants-2004_01
ORD IDord-d0a5427a349f432d86821072c7f1f785
Source noteuspto-grants-2004_01