Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329044Generated: October 26, 2026

Triethylamine → Flupimazine

https://huagongshe.com/reaction/329044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
Reactant2-(Piperidin-4-yloxy)ethan-1-olHCID 20295332—
SolventSodium IodideHCID 5238—
SolventMethyl Ethyl KetoneHCID 6569—
ProductFlupimazineHCID 218089—

Reaction Steps

40 g of 2-trifluoromethyl-10-(3-chloropropyl)-phenothiazine were dissolved in 350 ml of methyl ethyl ketone and 17.6 g of sodium iodide, 11.8 g of triethylamine, then 17 g of 2-(4-piperidyloxy)-ethanol were successively added to this solution. It was refluxed for 20 hours and after cooling, the precipitate was removed by vacuum filtration. The filtrate was evaporated to dryness to obtain 2-trifluoromethyl-10-[3-(4-β-hydroxyethoxypiperidino)-propyl]-phenothiazine as an oil which was added to a mixture of ether and dilute hydrochloric acid. The formed precipitate was recovered by vacuum filtration and was crystallized from 95% ethanol to obtain 40.5 g of 2-trifluoromethyl-10-[-3(4-β-hydroxyethoxypiperidino)-propyl]-phenothiazine hydrochloride as white crystals. Then a current of ammonia was led into an ether suspension of this product and the formed precipitate was removed by filtration. The filtrate was evaporated to dryness to obtain 2-trifluoromethyl-10-[3-(4-β-hydroxyethoxypiperidino)-propyl]-phenothiazine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04018922
Source datasetuspto-grants-1977_04
ORD IDord-44caedd389744c3aa62118cfbc87512f
Source noteuspto-grants-1977_04