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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495668Generated: October 30, 2026

Sulfuric Acid → HCID 22327975, compound

https://huagongshe.com/reaction/495668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-5-bromopyrimidineHCID 231310—
Reactant2-Fluorophenylboronic acidHCID 2734354—
CatalystHCID 178418397HCID 178418397—
SolventHexaneHCID 8058—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22327975HCID 22327975—

Reaction Steps

To a solution of 2-amino-5-bromo-pyrimidine 9 (49.40 g, 284 mmol) in dimethoxyethane (500 mL) were added 2-fluorophenylboronic acid 10 (43.66 g, 312 mmol), 2.0 M aqueous sodium carbonate solution (285 mL, 570 mmol) and tetrakis(triphenylphosphine)palladium (0) (3.28 g, 2.84 mmol). The mixture was stirred at reflux for 2 hr. The reaction mixture was cooled to ambient temperature and slowly poured into 10% H2SO4 (600 mL), which was added with hexane (300 mL). The acidic aqueous layer was separated, and the insoluble material and the organic layer was extracted with 10% H2SO4 (200 mL×2). The combined acidic aqueous layers were washed with EtOAc (200 mL), neutralized with K2CO3 to give a precipitate of the title compound and an inorganic salt, which were washed with water (3000 mL) to afford the title compound 11 as a white solid. The white solid was dissolved in hot THF (500 mL). The insoluble material was filtered off and concentrated in vacuo. The residual solid was washed with IPE to afford the title compound 11 as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939966B2
Source datasetuspto-grants-2005_09
ORD IDord-019c6ff289584c8f91e6bd396ce4ece5
Source noteuspto-grants-2005_09