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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356184Generated: November 3, 2026

Benzoyl bromide → HCID 18507507, compound

https://huagongshe.com/reaction/1356184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl bromideHCID 12056—
ReactantHCID 18507303HCID 18507303—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 18507507HCID 1850750730.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 200 mg (0.62 mmol) 2-amino-4-furan-2-yl-6-(2-pyridin-2-yl-ethylsulfanyl)-pyrimidine-5-carbonitrile and 8 mg (0.06 mmol) 4-dimethylaminopyridine in 2 ml pyridine was added dropwise 0.73 ml (6.18 mmol) benzoyl bromide and the reaction mixture stirred at 50° C. for 3 hours. The reaction mixture was then cooled to room temperature and partitioned between water and ethyl acetate. The combined organic phases were dried with sodium sulfate and concentrated in vacuo. Chromatography (1/2 ethyl acetate/hexane then 1/1 ethyl acetate/hexane then ethyl acetate) followed by trituration in ether afforded 100 mg (30%) N-benzoyl-N-[5-cyano-4-furan-2-yl-6-(2-pyridin-2-yl-ethylsulfanyl)-pyrimidin-2-yl]-benzamide as a white crystalline solid. ES-MS m/e (%): 532 (M+H+, 68).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586441B2
Source datasetuspto-grants-2003_07
ORD IDord-6f4bfdde7d8c4038a638be5f6dccf09a
Source noteuspto-grants-2003_07