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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762126Generated: November 3, 2026

Ethyl chloroformate → Deschloro Loratadine

https://huagongshe.com/reaction/1762126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantAzatadineHCID 19861—
SolventBenzeneHCID 241—
ProductDeschloro LoratadineHCID 12884174—

Reaction Steps

To a solution of 10.9 g (0.1 mole) of ethylchloroformate in 300 ml of anhydrous benzene is added dropwise, with stirring at room temperature, a solution of 14.5 g (0.05M) of 11-(N-methyl-4-piperidylidene)-6,11-dihydro-5H-benzo-[5,6]-cyclohepta[1,2-b]-pyridine (hereinafter referred to as Compound IA) in 200 ml of benzene. The solution is stirred and is heated under reflux overnight (16-20 hrs.). The mixture is cooled and is poured into ice water and the organic layer is separated, washed with water, dried, and then concentrated to dryness. The residue is triturated with petroleum ether and a white solid having a melting point of 106°-107° C. is recrystallized from isopropyl ether after decolorization with decolorizing carbon.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831042
Source datasetuspto-grants-1989_05
ORD IDord-36e7ea441b1144a4a0285b9621949f1b
Source noteuspto-grants-1989_05