Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407429Generated: October 30, 2026

2-Chloro-5-iodopyridin-4-amine → HCID 59578429, compound

https://huagongshe.com/reaction/2407429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-iodopyridin-4-amineHCID 45480366—
ReactantMethyl 5-ethynylnicotinateHCID 53898384—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 59578429HCID 59578429—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 250 mL round bottom flask flushed with N2 was charged with 2-chloro-5-iodo-pyridin-4-ylamine (1.00 g, 3.93 mmol), 5-ethynyl-nicotinic acid methyl ester (0.633 g, 3.93 mmol), copper(I) iodide (0.037 g, 0.196 mmol), bis(triphenylphosphine)palladium(II) chloride (0.138 g, 0.196 mmol) and triethyl amine (50 mL). The reaction mixture was stirred at 100° C. for 3 h. The reaction was cooled to room temperature, filtered and the precipitate washed thoroughly with ethyl acetate. The filtrate was washed with water twice. The organic layer was dried over sodium sulfate and concentrated in vacuo to afford crude product 5-(4-amino-6-chloro-pyridin-3-ylethynyl)-nicotinic acid methyl ester as a brown solid which was taken onto next step without any purification. ESI-MS: m/z 288.0 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809545B2
Source datasetuspto-grants-2014_08
ORD IDord-5fe1f6d1f47244ddadd5262f4425b9e2
Source noteuspto-grants-2014_08