HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882163Generated: October 31, 2026
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → HCID 89615759, compound
https://huagongshe.com/reaction/882163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 2-(Tri-n-butylstannyl)oxazole | HCID 15486183 | — |
| Reactant | HCID 89629894 | HCID 89629894 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 89615759 | HCID 89615759 | — |
Reaction Steps
To a solution of N-(3-(5-bromo-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)methacrylamide (249 mg, 0.51 mmol) in toluene (10 mL) under nitrogen, was added 2-(tributylstannyl)-1,3-oxazole (548 mg, 1.53 mmol), Pd2(dba)3 (93 mg, 0.10 mmol), and X-Phos (95 mg, 0.20 mmol). The resulting solution was stirred overnight at 60° C. and then concentrated in vacuo, and the resulting crude reaction was extracted with ethyl acetate (×3). The combined organic layers were washed with brine, dried with anhydrous sodium sulfate, filtered and concentrated in vacuo. The reaction was then purified by chromatography using silica gel, eluting with 0-100% EtOAc/petroleum ether. The product was collected and concentrated in vacuo to afford N-(3-(5-(oxazol-2-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)methacrylamide as a yellow oil. LRMS (ESI) calc'd for C25H30N5O3Si [M+H]+: 476, found 476.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08993756B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-357415ecf4b742b48a902b8cc1bd56e3 |
|---|
| Source note | uspto-grants-2015_03 |
|---|