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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764219Generated: November 4, 2026

Phenothiazine → HCID 20307176, compound

https://huagongshe.com/reaction/1764219

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 off 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 numberUS04115571
Source datasetuspto-grants-1978_09
ORD IDord-dfd6b3302b0745c79a289bf92d0c17c8
Source noteuspto-grants-1978_09