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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917717Generated: November 3, 2026

Propargyl alcohol → HCID 11255499, compound

https://huagongshe.com/reaction/917717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantHCID 11338183HCID 11338183—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductHCID 11255499HCID 1125549989%

Reaction Steps

4-(2-Fluoro-4-iodoanilino)-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamide was reacted with propargyl alcohol in the presence of CuI, (Ph3P)2PdCl2 and TEA in DMF as for example 2. The residue resulting from removal of the reaction solvents under reduced pressure was purified by column chromatography on silica gel (5% MeOH/CH2Cl2 as eluant) to give 4-[2-fluoro-4-(3-hydroxy-1-propynyl)anilino]-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxamide as an off-white solid (89%). 1H NMR [(CD3)2SO, 400 MHz] δ 10.57 (s, 1 H), 8.35 (s, 1H), 7.90 (br s, 1H), 7.50 (t, J=8.5 Hz, 1H), 7.48 (br s, 1H), 7.39 (dd, J=11.4, 1.8 Hz, 1H), 7.28 (dd, J=8.3, 1.5 Hz, 1H), 5.69 (s, 1H), 5.36 (t, J=6.0 Hz, 1H), 4.30 (d, J=5.9 Hz, 2H), 3.37 (s, 3H). LCMS (APCI+) calcd for C16H15FN3O3 316 (MH+), found 316.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273877B2
Source datasetuspto-grants-2007_09
ORD IDord-aa5f858d30a048698d69fcf13c7dce87
Source noteuspto-grants-2007_09