HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-fluoro-4,5-dimethylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trimethylboroxine | HCID 574072 | — |
| Reactant | 3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-fluoro-4-iodo-5-methylpyridine | HCID 23082581 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-fluoro-4,5-dimethylpyridine | HCID 23082585 | 70.3% |
Reaction Steps
1.50 g (3.37 mmol) of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-2-fluoro-4-iodo-5-methylpyridine obtained in Step (c), 1.40 g (10.1 mmol) of potassium carbonate, 0.39 g (0.34 mmol) of tetrakis(triphenylphosphine)palladium, 15 ml of dioxane and 0.42 g (1.67 mmol) of 50% trimethylboroxin were mixed, followed by reflux with heating for 6 hours. After cooling to room temperature, filtration on the pad of celite and washing with ethyl acetate and tetrahydrofuran were carried out, the solvent was distilled off under reduced pressure, and the obtained crude product was purified by silica gel chromatography to obtain 0.79 g (yield: 70%) of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-2-fluoro-4,5-dimethylpyridine (Compound No. 19).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653277B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-bfda7531ef0c4a7e801ce26b30b13a37 |
| Source note | uspto-grants-2014_02 |