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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant2-(Tri-n-butylstannyl)oxazoleHCID 15486183—
ReactantHCID 89629894HCID 89629894—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 89615759HCID 89615759—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993756B2
Source datasetuspto-grants-2015_03
ORD IDord-357415ecf4b742b48a902b8cc1bd56e3
Source noteuspto-grants-2015_03