HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → 2-(2-Chlorophenylamino)-3,4-difluoro-6-trimethylsilanylethynylbenzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 6-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl ester | HCID 86598592 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Chlorophenylamino)-3,4-difluoro-6-trimethylsilanylethynylbenzoic acid methyl ester | HCID 86598593 | 79% |
Reaction Steps
A mixture of 6-bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl ester (2.61 g, 6.93 mmol), TMS-acetylene (1.18 mL, 8.32 mmol), Pd(PPh3)2Cl2 (496 mg, 0.693 mmol), CuI (132 mg, 0.693 mmol), and i-Pr2NH (1.95 mL, 13.9 mmol) in THF (11 mL) was stirred for 16 hours at room temperature. The reaction mixture was concentrated in vacuo, diluted with EtOAc, and washed with saturated aqueous NH4Cl and brine. The organic layer was dried over MgSO4, filtered, and concentrated to give the crude material that was purified by silica gel flash column chromatography (100% hexanes to 1% to 2% EtOAc in hexanes) to afford the desired product (2.15 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07485643B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-a9b26cc0fdfc4ec18e9feb4226bbfb3d |
| Source note | uspto-grants-2009_02 |