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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977927Generated: October 25, 2026

Triethylamine → Lomerizine Hydrochloride

https://huagongshe.com/reaction/977927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimetazidine DihydrochlorideHCID 83201—
Reactant1,1'-(Chloromethylene)bis(4-fluorobenzene)HCID 2723773—
SolventO-XyleneHCID 7237—
ProductLomerizine HydrochlorideHCID 12212522.1%

Reaction Steps

2.4 g (7.1 millimoles) of 2,3,4-trimethoxybenzylpiperazine dihydrochloride, 1.8 g (7.5 millimoles) of bis(4-fluorophenyl)methyl chloride [see J. Chem. Soc. Perkin II, 1051 (1977)] and 5.0 ml (36 millimoles) of triethylamine were heated under reflux for 9 hours in 80 ml of xylene. The reaction mixture was allowed to cool to room temprature, 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 0.85 g of 1-(2,3,4-trimethoxybenzyl)-4-[bis(4-fluorophenyl)methyl]piperazine dihydrochloride. 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-a4e6364165b44ee2a74c0e6e9f851403
Source noteuspto-grants-1987_05