HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329045Generated: October 26, 2026
Triethylamine → 2-Trifluoromethyl-10-[3-(4-beta-{2-methylheptanoyloxy}ethoxypiperidino)-propyl]-phenothiazine
https://huagongshe.com/reaction/329045
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Flupimazine | HCID 218089 | — |
| Reactant | 2-Methylheptanoyl chloride | HCID 14234519 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Trifluoromethyl-10-[3-(4-beta-{2-methylheptanoyloxy}ethoxypiperidino)-propyl]-phenothiazine | HCID 53721547 | 30% |
Reaction Steps
13.55 g of 2-trifluoromethyl-10-[3-(4-β-hydroxyethoxypiperidino)-propyl]-phenothiazine (prepared by Example XLIII), 5.4 ml of triethylamine and 100 ml of anhydrous benzene were added to a flask and a solution of 5.7 g of 2-methyl-heptanoic acid chloride in 50 ml of anhydrous benzene was added thereto. The mixture was agitated at room temperature for 24 hours and then the precipitate formed was removed by filtration. The benzene filtrate was washed with an aqueous solution of sodium bicarbonate, then with water. After drying and concentration of the benzene solution, the resulting oil was purified by chromatography on silica gel. After elution with ethanol and evaporation of the solvent, 5.2 g of 2-trifluoromethyl-10-[3-(4-β-{2-methylheptanoyloxy}ethoxypiperidino)-propyl]-phenothiazine as a clear oil were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04018922 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-f1c30b42051d48ec83d999ce52d27245 |
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| Source note | uspto-grants-1977_04 |
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