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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678856Generated: November 2, 2026

Phenothiazine → HCID 20307176, compound

https://huagongshe.com/reaction/1678856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenothiazineHCID 7108—
ReactantPotassium HydroxideHCID 14797—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5-Methyl-2-pyrrolidoneHCID 66055—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 20307176HCID 2030717617%

Reaction Steps

A mixture of 5-methyl-2-pyrrolidinone (6.0 g., 0.06 mole), phosphorus oxychloride (9.2 g., 0.06 mole) in 60 ml. of 1,2-dichloroethane is refluxed for 10 min. A solution of phenothiazine (6.0 g., 0.03 mole) in 20 ml. of 1,2-dichloroethane is added at the end of the reflux period and the reaction mixture stirred and refluxed for 20 hr., and then poured onto 20 ml. of 5N potassium hydroxide and 20 g. of crushed ice. The 1,2-dichloroethane layer is separated and extracted with 30 ml. of 1.5N hydrochloric acid and 30 ml. of water removing water soluble by-product 10-[2-(5-methyl-1-pyrrolinyl)]phenothiazine hydrochloride. After drying the 1,2-dichloroethane solution over magnesium sulfate, the 1,2-dichloroethane solution is concentrated and the solid thus obtained stirred with 40 ml. of acetone and filtered. Crystallization of the filtercake from ethanol-ether provides analytically pure 10-[5-METHYL-1-(5-METHYL-1-PYRROLIN-2-YL)-2-PYRROLIN-2-YL]PHENOTHIAZINE HYDROCHLORIDE in a yield of 17%, m.p. 257°-264° C. (corr.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04077959
Source datasetuspto-grants-1978_03
ORD IDord-0b6523d7a2bb4f3ab3f87c3c5347ed42
Source noteuspto-grants-1978_03