HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 86720174, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Hydroxybenzonitrile | HCID 11907 | — |
| Reactant | HCID 10682881 | HCID 10682881 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86720174 | HCID 86720174 | — |
Reaction Steps
To the suspension of the acid chloride of 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylic acid (4 mmol) obtained according to Pochet et al. (Bioorg. Med. Chem. 2000, 8, 1489) in anhydrous dioxane (10 mL) was added 2-cyanophenol (5 mmol) and pyridine (0.4 mL). After 12 h stirring at room temperature, the solvent was evaporated under vacuum and the residue was suspended in methanol. The resulting precipitate was collected by filtration, washed with methanol and dried. The solid was crystallyzed in ethyl acetate (40%); mp: 181-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006466B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-12a459facdcc4cd698eb2eae88fe7457 |
| Source note | uspto-grants-2015_04 |