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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977926Generated: October 26, 2026

Triethylamine → Lomerizine Hydrochloride

https://huagongshe.com/reaction/977926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantToluene, alpha-chloro-2,3,4-trimethoxy-HCID 97491—
Reactant1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
SolventBenzeneHCID 241—
ProductLomerizine HydrochlorideHCID 12212598.5%

Reaction Steps

1.3 g (6.0 millimoles) of 2,3,4-trimethoxybenzyl chloride [see Monatsh., 95 (3), 942 (1964)], 1.7 g (5.9 millimoles) of bis(4-fluorophenyl)methylpiperazine and 1.2 ml (8.6 millimoles) of triethylamine were heated under reflux for 6 hours in 50 ml of benzene. The reaction mixture was allowed to cool to room temperature, washed with water, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. A mixture of 2 ml of conc. hydrochloric acid and 20 ml of ethanol was added to the resulting oily product, and the mixture was concentrated under reduced pressure. Ether was added, and the precipitated crystals were collected by filtration. Recrystallization of the crystals from ethanol-ether gave 1.6 g of 1-(2,3,4-trimethoxybenzyl)-4-[bis(4-fluorophenyl)methyl]piperazine dihydrochloride as colorless crystals. The product showed the same property values as the compound obtained in Example 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663325
Source datasetuspto-grants-1987_05
ORD IDord-d166fb5bb6d94b9793f7aadc19477feb
Source noteuspto-grants-1987_05