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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299258Generated: October 30, 2026

Water → 8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one

https://huagongshe.com/reaction/2299258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhosphorus oxychlorideHCID 24813—
Reactantn-Phenyl-3-[2-(3chlorophenyl)ethyl]-2-pyridine carboxamideHCID 9862612—
SolventChlorobenzeneHCID 7964—
Product8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-oneHCID 9816260—

Reaction Steps

A mixture of trifluroromethanesulfonic acid (63.2 ml; 0.71 mol) and phosphorus oxychloride (66.4 ml; 0.71 mol) in chlorobenzene (400 ml) was stirred for ½hour at room temperature. A solution of N-phenyl-3-[2-(3-chlorophenyl)ethyl]-2-pyridine carboxamide 4 (120 g; 0.36 mol) in chlorobenzene (240 ml) was added. The mixture was heated at 110° C. for 18 hours followed by cooling to 50° C. Water (400 ml) was added and the biphasic mixture heated to 80° C. for ½ hour. The mixture was cooled to room temperature, stirred vigorously for 10 minutes, then allowed to stand for 10 minutes. The product was removed by filtration and partitioned between water (300 ml) and toluene (500 ml). The pH of the aqueous phase was adjusted to 10 with 10M NaOH solution. 100 ml of the organic phase was removed by distillation under reduced pressure. Charcoal (5.5 g) was added and the mixture filtered through a pad of celite. The solution was concentrated under vacuum to 300 ml and 150 ml of hexane was added. The mixture was cooled to 0-10° C. for 1 hour with stirring prior to filtration. The product was washed with 100 ml of chilled toluene and then air-dried for several hours. Yield 44.1 g (50.8%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495689B2
Source datasetuspto-grants-2002_12
ORD IDord-6f0d946857634e1bbd8e5ca1d2906c9e
Source noteuspto-grants-2002_12