HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044015Generated: October 30, 2026
Ethynylcyclobutane → HCID 57908178, compound
https://huagongshe.com/reaction/1044015
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethynylcyclobutane | HCID 142749 | — |
| Reactant | tert-Butyl (6-chloro-4-iodopyridin-3-yl)carbamate | HCID 53415320 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 57908178 | HCID 57908178 | 60% |
Reaction Steps
To the solution of tert-butyl 6-chloro-4-iodopyridin-3-ylcarbamate (7.0 g, 19.8 mmol) in Et3N (100 mL) was added the solution of ethynylcyclobutane in THF (prepared in step a), Pd(PPh3)2Cl2 (1.8 g, 2.1 mmol) and CuI (400 mg, 2.1 mmol). The reaction mixture was stirred at 25° C. for 16 h. The mixture was diluted with water and extracted with dichloromethane (3×100 mL). The extract was washed with brine, dried, concentrated in vacuo and purified by chromatography on silica gel (5-10% ethyl acetate in petroleum ether as eluant) to afford tert-butyl 6-chloro-4-(cyclobutylethynyl)pyridin-3-ylcarbamate (3.6 g, 60% yield). 1H NMR (300 MHz, CDCl3) δ: 9.11 (br, s, 1H), 7.22 (s 1H), 6.97 (s, 1H), 3.39-3.25 (m, 1H), 2.48-1.98 (m, 6H), 1.52 (s, 9H).
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-d78b6778637f40f4962bf3956da92f55 |
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| Source note | uspto-grants-2013_10 |
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