HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201013Generated: October 28, 2026
Triphenylphosphine → HCID 86663078, compound
https://huagongshe.com/reaction/2201013
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Methoxyphenylboronic acid | HCID 2733958 | — |
| Reactant | 2-Chloro-5-iodopyridin-4-amine | HCID 45480366 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 86663078 | HCID 86663078 | 80.5% |
Reaction Steps
Potassiumphosphate (18.28 g, 79 mmol), triphenyl phosphine (1.04 g, 3.97 mmol), 2-chloro-5-iodo-4-aminopyridine (10.1 g, 39. mmol), 2-methoxybenzeneboronic acid (8.44 g, 55.57 mmol) and palladium acetate (0.45 g, 1.98 mmol) were sequentially added to degassed acetonitrile (300 mL) and water (100 mL) under nitrogen. The reaction mixture was heated at 75° C. for overnight, then cooled to room temperature. The organic layer was separated and aqueous layer and was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated and performed column chromatography using hexanes and ethyl acetate as eluent. 7.5 g of title compound was isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359549B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-5f08475a938642769fb31de21fbb3332 |
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| Source note | uspto-grants-2016_06 |
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