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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262828Generated: November 1, 2026

Ethyl chloroformate → Deschloro Loratadine

https://huagongshe.com/reaction/1262828

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 numberUS04454143
Source datasetuspto-grants-1984_06
ORD IDord-72a11341fee04634aa36d2ea5a433a31
Source noteuspto-grants-1984_06