HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365819Generated: October 31, 2026
4-Vinylpyridine → HCID 54192486, compound
https://huagongshe.com/reaction/365819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Vinylpyridine | HCID 7502 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22872668 | HCID 22872668 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 54192486 | HCID 54192486 | — |
Reaction Steps
To a solution of 5-bromo-6-chloro-3-(1-BOC-2-(S)-pyrrolidinylmethoxy)pyridine added 4-vinylpyridine (156 mg, 1.5 mmol), palladium acetate (29.0 mg, 0.12 mmol), tri-o-tolylphosphine (156 mg, 0.12 mmol) and triethylamine (3.2 mL). The reaction mixture was heated in a sealed tube at 100° C. overnight, then cooled to room temperature. Minimum amount of saturated sodium bicarbonate was added to free the amine hydrochloride salt, and the mixture was extracted with EtOAc, dried (MgSO4), and concentrated. The residue was chromatographed on a silica gel column, eluting with 4 to 50% Et2O in hexane) to give the title compound (282 mg). MS (CI/NH3) m/z 416 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127386 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-161236eac804499fa0a640e48a9df672 |
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| Source note | uspto-grants-2000_10 |
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