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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109533Generated: October 30, 2026

Acetic Acid → N-propyl-10-[1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide

https://huagongshe.com/reaction/1109533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 14536531HCID 14536531—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-propyl-10-[1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamideHCID 9800851—

Reaction Steps

Mercuric acetate (0.38 g) is added with stirring to a solution of N-propyl-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbothioamide neutral fumarate (0.6 g) in acetic acid (10 cc), and stirring is continued for 4 hours 30 minutes at a temperature in the region of 20° C. The black reaction mixture is diluted with distilled water (25 cc) and ethyl acetate (50 cc) and then filtered and alkalinized with stirring with 4N aqueous sodium hydroxide solution to pH 13. After settling has taken place, the organic phase is separated and the aqueous phase is extracted with ethyl acetate (20 cc). The combined organic phases are washed successively with saturated aqueous sodium chloride solution (50 cc). After drying over magnesium sulphate, filtration and concentration to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C., N-propyl-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide (0.43 g) is obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05321026
Source datasetuspto-grants-1994_06
ORD IDord-348a9474552d443fa785dfbba254f2ca
Source noteuspto-grants-1994_06