HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201016Generated: October 29, 2026
Triphenylphosphine → HCID 86663080, compound
https://huagongshe.com/reaction/2201016
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Methoxyphenylboronic acid | HCID 2733958 | — |
| Reactant | 6-Chloro-5-iodopyridin-2-amine | HCID 70700961 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 86663080 | HCID 86663080 | 71.9% |
Reaction Steps
Potassium phosphate (12.72 g, 60 mmol), triphenyl phosphine (0.682 g, 2.40 mmol), 6-chloro-5-iodo-2-aminopyridine (6.1 g, 24 mmol), 2-methoxybenzeneboronic acid (5.10 g, 33.5 mmol) and palladium acetate (0.27 g, 1.20 mmol) were sequentially added to degassed acetonitrile (200 mL) and water (60 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 purified by silica column using hexanes and ethyl acetate as eluent furnishing 4.05 g of title compound.
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-afb4646395c1452f832fe7ea2fb73afd |
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| Source note | uspto-grants-2016_06 |
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