Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647996Generated: October 25, 2026

Phosphorus oxychloride → Isopropyl 3-p-fluorobenzoyl-5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylate

https://huagongshe.com/reaction/647996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-fluoro-N,N-dimethylbenzamideHCID 141077—
ReactantIsopropyl 5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylateHCID 12795102—
ReactantSodium Acetate TrihydrateHCID 23665404—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductIsopropyl 3-p-fluorobenzoyl-5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylateHCID 20484013—

Reaction Steps

A solution of 758 mg. of N,N-dimethyl-4-fluorobenzamide and 0.44 ml. of phosphorous oxychloride in 50 ml. of 1,2-dichloroethane is refluxed for one hour. To this solution is added a solution of 500 mg. of isopropyl 5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylate in 10 ml. 1,2-dichloroethane. The reaction mixture is refluxed for 3 hours. A solution of 3.3 g. sodium acetate trihydrate in 9 ml water is added and refluxed for a further 10 hours. The organic phase is separated, washed with saturated sodium chloride solution, dried over sodium sulfate and evaporated to dryness. The residue is purified by preparative t.l.c. using hexane:ethyl acetate (90:10). Crystallization from dichloromethane-hexane yields isopropyl 3-p-fluorobenzoyl-5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylate (XI, R=H, L=p-F, R2 =iC3H7, n=1), m.p. 92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410534
Source datasetuspto-grants-1983_10
ORD IDord-cc16e4974dda462b8218d8903d8cfca0
Source noteuspto-grants-1983_10