HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11949616, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Trifluoromethyl)benzoyl chloride | HCID 67561 | — |
| Reactant | HCID 63317696 | HCID 63317696 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11949616 | HCID 11949616 | 32.4% |
Reaction Steps
To 0.06 g of 2-(5-bromopyrimidin-2-yl)ethanamine (3.0 mmol) and triethylamine (0.03 g, 1.0 equivalent) in THF (5 ml), at room temperature whilst stirring, was added the 2-trifluoromethyl benzoyl chloride (0.062 g, 1.0 equivalent) and the mixture was left to stir at room temperature overnight. The solvent was removed by evaporation in vacuo and saturated sodium bicarbonate (10 mls) was added. The mixture was extracted with dichloromethane and the organic phase was collected, dried over MgSO4, and evaporated in vacuo to give the crude product which was purified by chromatography on silica using 1:1 heptane/ethyl acetate to yield to 0.036 g of N-[2-(5-bromopyrimidin-2-yl)ethyl]-2-(trifluoromethyl)benzamide (Compound A-1) (32%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960391B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-e3a87bdb6ccb47abae1c73fd50e3d20b |
| Source note | uspto-grants-2011_06 |