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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657603Generated: November 3, 2026

4-Piperidineethanol → HCID 21534829, compound

https://huagongshe.com/reaction/1657603

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PiperidineethanolHCID 73953—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21534822HCID 21534822—
SolventDimethylformamideHCID 6228—
ProductHCID 21534829HCID 2153482973.2%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 2-heptyloxy-6-dimethylsulphamoyl-10-(3-chloropropyl)phenothiazine (24.3 g.), 4-hydroxyethylpiperidine (7.1 g.) and sodium bicarbonate (16.1 g.) in dimethylformamide (180 cc.) is heated at about 130°C. for 8 hours with stirring. After cooling, the reaction mixture is evaporated to dryness under reduced pressure (15 mm.Hg) with heating to 65°C. The residue is taken up in distilled water (300 cc.) and then extracted with methylene chloride (total 560 cc.). The combined organic extracts are acidified by addition of a solution of methanesulphonic acid (57.6 cc.) in water (250 cc.). The organic phase is washed with an 8% aqueous solution of sodium hydroxide (total 300 cc.) and then with distilled water (total 1 litre), and is finally dried over sodium sulphate. On evaporation of the solvent under reduced pressure (15 mm. Hg) at 40°C., crude 2-heptyloxy-6-dimethylsulphamoyl-10-[3-(4-hydroxyethylpiperidino)propyl]-phenothiazine (21.1 g.), in the form of a brown viscous oil, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03961055
Source datasetuspto-grants-1976_06
ORD IDord-dddfb84a941548e199e006d8a8c4bd14
Source noteuspto-grants-1976_06