HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897801Generated: October 31, 2026
2-Chloro-5-iodopyridin-4-amine → HCID 59578429, compound
https://huagongshe.com/reaction/1897801
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-5-iodopyridin-4-amine | HCID 45480366 | — |
| Reactant | Methyl 5-ethynylnicotinate | HCID 53898384 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 59578429 | HCID 59578429 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519142B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-9eeb1f981be048809cab03faaa19b75b |
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| Source note | uspto-grants-2013_08 |
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