HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044012Generated: October 25, 2026
6-Chloro-4-iodopyridin-3-amine → 6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amine
https://huagongshe.com/reaction/1044012
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Chloro-4-iodopyridin-3-amine | HCID 18407040 | — |
| Reactant | 1-Ethynyl-1-methylcyclopropane | HCID 21590560 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amine | HCID 57908192 | 53% |
Reaction Steps
To a solution of 6-chloro-4-iodopyridin-3-amine (7.0 g, 28 mmol) in Et3N (100 mL) was added 1-ethynyl-1-methyl-cyclopropane (11.0 g, 137 mmol), CuI (0.53 g, 2.8 mmol) and Pd(PPh3)2Cl2 (1.9 g, 2.8 mmol) under N2 atmosphere. The mixture was refluxed overnight and quenched with H2O (100 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (100 mL×3). The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and purified by chromatography on silica gel (3% EtOAc in Petroleum ether as eluant) to afford 6-chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amine (3.0 g, 53%). 1H-NMR (CDCl3, 300 MHz) δ 7.84 (s, 1H), 7.08 (s, 1H), 4.11 (br s, 2H), 1.37 (s, 3H), 1.03 (t, J=2.4, 2H) 0.76 (t, J=2.4, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563573B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-f3f87881eed3484082014f791528b3ae |
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| Source note | uspto-grants-2013_10 |
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