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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53128Generated: October 29, 2026

Pyridine → HCID 15205142, compound

https://huagongshe.com/reaction/53128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromineHCID 24408—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHCID 19961812HCID 19961812—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
ProductHCID 15205142HCID 1520514249.2%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a 200 mL three neck round-bottomed flask equipped with a nitrogen inlet and septum were added 5.48 grams (21.8 mmol) 5-phenyl-8-methyl-2-oxobenzazepine, 100 mL dichloromethane, and 4.55 grams (21.8 mmol) phosphorus pentachloride. After dissolution, 1.85 mL (22.9 mmol) pyridine was added, and the solution cooled to -70° C. To the stirring solution (some precipitate appeared at this temperature, but did not affect the reaction) was added a solution of 1.12 mL (21.8 mmol) bromine in 10 mL methylene chloride dropwise over 20 minutes. The reaction was then allowed to warm quickly (10 minutes) to 0° C., and 50 mL of saturated aqueous sodium bisulfite solution was added. The reaction was then diluted with methylene chloride and allowed to stand under sodium bisulfite solution with periodic shaking for 2 hours, until the organic phase no longer exhibited a reddish color. The organic phase was then dried over sodium sulfate and evaporated. The residue was suspended in methylene chloride and filtered, and the solid dissolved to afford 3.39 grams (47%) of product as a white solid. The filtrate was adsorbed onto silica gel and chromatographed using 7:3 hexane/ethyl acetate as eluant to afford additional product as a white solid, 1.38 g, total 5.14 (71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618811
Source datasetuspto-grants-1997_04
ORD IDord-95f6d3ee9a0b49bfab7126a901e7f652
Source noteuspto-grants-1997_04