HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → [6-Amino-5-(trifluoromethyl)pyridin-3-yl]boronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | 5-Bromo-3-(trifluoromethyl)pyridin-2-amine | HCID 20525383 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | [6-Amino-5-(trifluoromethyl)pyridin-3-yl]boronic acid | HCID 53407570 | — |
Reaction Steps
5-bromo-3-(trifluoromethyl)pyridin-2-amine (9.85 mmol, commercially available), Bis(pinacolato)diboron (11.82 mmol), potassium acetate (1.4 g) and (1,1-bis(diphenylphosphino)ferrocene)-dichloropalladium (II) complex with DCM (200 mg, commercially available) was dissolved in dioxane (75 mL) under argon atmosphere. The reaction mixture was refluxed for 8 h. The reaction mixture was cooled, diluted with ethyl acetate (75 mL) and filtered. The filtrate was concentrated. The crude product was purified over silica gel using 0-10% ethyl acetate in petroleum ether to obtain the titled boronic acid derivative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062046B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-e4a56016496947f6bacc45c5abcb4431 |
| Source note | uspto-grants-2015_06 |