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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391317Generated: October 30, 2026

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

https://huagongshe.com/reaction/391317

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 numberUS08383827B2
Source datasetuspto-grants-2013_02
ORD IDord-e01a748df14948058b125d1ebfc03ec4
Source noteuspto-grants-2013_02