HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548554Generated: October 24, 2026
1-(Prop-2-yn-1-yl)piperidine → HCID 67157959, compound
https://huagongshe.com/en/reaction/548554
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Prop-2-yn-1-yl)piperidine | HCID 336652 | — |
| Reactant | {4-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acid methyl ester | HCID 67157962 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 67157959 | HCID 67157959 | — |
Reaction Steps
A mixture of 1-prop-2-ynyl-piperidine (53 mg, 0.44 mmol), {4-[3-(3,5-dibromo-phenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acid methyl ester (204 mg, 0.44 mmol, intermediate 2), Pd(PPh3)4 (50 mg, 0.044 mmol), CuI (23 mg, 0.12 mmol) in dry DMF (2 ml) and triethylamine (2 ml) was heated in a microwave own for 30 min at 60° C. in a sealed tube. The reaction mixture was filtered through Decalite and the filtrate was evaporated. The residue was purified on column chromatography using ethyl acetate/methanol mixtures to give (4-{3-[3-bromo-5-(3-piperidin-1-yl-prop-1-ynyl)-phenyl]-prop-2-ynyloxy}-2-methyl-phenoxy)-acetic acid methyl ester in 105 mg (47%) yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943612B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-c133269f32754ccf9df637f82283c00e |
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| Source note | uspto-grants-2011_05 |
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