HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 59305023, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-4-nitroaniline | HCID 101254 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 4-Chloro-3-(trifluoromethyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrrolo[2,3-b]pyridine | HCID 59304981 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 59305023 | HCID 59305023 | — |
Reaction Steps
A solution of 170 mg (0.485 mmol) of 4-chloro-3-(trifluoromethyl)-1-{[2-(trimethylsilyl)ethoxy]-methyl}-1H-pyrrolo[2,3-b]pyridine, 91 mg (0.58 mmol) of 2-fluoro-4-nitroaniline, 31 mg (0.035 mmol) of tris(dibenzylideneacetone)dipalladium, 33 mg (0.07 mmol) of dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine and 100 mg (0.72 mmol) of potassium carbonate in 3.00 ml of degassed tert-butanol is stirred in a sealed pressure vessel at 100° C. for 3 h. After cooling to RT, the reaction mixture is filtered through kieselguhr, the kieselguhr is washed with ethyl acetate and the filtrate is freed from the solvent. The residue is purified by preparative HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723347B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-e07a1f1b6d7c4804ab5e798cefd779a7 |
| Source note | uspto-grants-2010_05 |