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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882127Generated: October 25, 2026

4-Bromopyrimidine-2-carbonitrile → Ethyl 4-(3-(2-cyanopyrimidin-4-yl)phenyl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

https://huagongshe.com/reaction/882127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromopyrimidine-2-carbonitrileHCID 53407910—
ReactantHCID 89629877HCID 89629877—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
ProductEthyl 4-(3-(2-cyanopyrimidin-4-yl)phenyl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylateHCID 89630128—

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of ethyl 4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate (54.4 mg, 0.104 mmol), 4-bromopyrimidine-2-carbonitrile (38.2 mg, 0.208 mmol), and tetrakis(triphenylphosphine)palladium(0) (24 mg, 0.021 mmol) in 2 M aqueous sodium carbonate (150 uL) and DME (500 μL) was purged with argon. The reaction vessel was then sealed and heated at 95° C. overnight. The reaction mixture was filtered through Celite and rinsed with ethyl acetate. The reaction solution was concentrated under reduced pressure and the residue purified by chromatography on silica eluting with 40-60% ethyl acetatehexane to give the desired product. LRMS calc'd for C26H29N6O3Si [M+H]+: 501, found 501.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993756B2
Source datasetuspto-grants-2015_03
ORD IDord-52b0886f08984b8583dca5ffd52fcb58
Source noteuspto-grants-2015_03