HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Phosphate, Tribasic → N-(6-Cyclopropyl-pyridin-2-yl)-2,2-dimethyl-propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | N-(6-Bromopyridin-2-yl)-2,2-dimethylpropanamide | HCID 9921361 | — |
| Catalyst | Tricyclohexylphosphine | HCID 75806 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene water | HCID 22272177 | — |
| Product | N-(6-Cyclopropyl-pyridin-2-yl)-2,2-dimethyl-propionamide | HCID 60019882 | 235.8% |
Reaction Steps
A mixture of N-(6-bromopyridin-2-yl)pivalamide (2 g, 7.77 mmol), cyclopropylboronic acid (935 mg, 10.88 mmol), potassium phosphate (toluene/water (10/3 mL) taken in screw cap tube was purged with argon for 15 minutes and then added palladium(II)acetate (174 mg, 0.77 mmol), tricyclohexylphosphine (435.7 mg, 1.55 mmol) sequentially, purged argon for another 5 min. The resultant mixture was stirred at 100° C. under closed argon atmosphere. Reaction completed in 14 h, reaction mass was cooled to room temperature, extracted into ethyl acetate, (100 ml) organic portion was washed with water, dried over sodium sulfate and concentrated to afford 4 g of the titled compound. LCMS: m/z=219.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353107B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-df770c310e90419dbc01dccaef5b7d06 |
| Source note | uspto-grants-2016_05 |