HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873752Generated: October 29, 2026
Cyclopropylacetylene → HCID 86724301, compound
https://huagongshe.com/reaction/873752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropylacetylene | HCID 138823 | — |
| Reactant | HCID 86724302 | HCID 86724302 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86724301 | HCID 86724301 | 15.6% |
Reaction Steps
To a stirred solution of di-tert-butyl [6′-(5-bromopyridin-3-yl)trispiro[cyclobutane-1,2′-chromene-4′,4″-[1,3]oxazole-3′,3′″-oxetan]-2″-yl]imidodicarbonate (48 mg, 0.075 mmol) in Et3N (0.67 ml) were added ethynylcyclopropane (0.063 mL, 0.75 mmol), PdCl2(PPh3)2 (10 mg, 0.015 mmol) and CuI (5.7 mg, 0.030 mmol) at room temperature and the mixture was sealed and irradiated with microwave at 150° C. for 1 hour. To this mixture was added activated carbon (ca. 100 mg) and the mixture was stirred for 1 hour to remove palladium residues. The mixture was passed through a pad of Celite. The filtrate was evaporated to give a residue. To the solution of the residue in toluene (3 ml) was added silica gel (500 mg) and the mixture was refluxed for 2 hours. The mixture was passed through a pad of Celite and the filtrate was evaporated to give a crude product, which was purified with column chromatography (MeOH in CHCl3=0 to 10%) to give 6′-[5-(cyclopropylethynyl)pyridin-3-yl]trispiro[cyclobutane-1,2′ chromene-4′,4″-[1,3]oxazole-3′,3′″-o xetan]-2″-amine (5 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975415B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-deb456ae479143929715e4a3bf3086e9 |
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| Source note | uspto-grants-2015_03 |
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