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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839902Generated: October 26, 2026

Promethazine Hydrochloride → Thiazinamium Metilsulfate

https://huagongshe.com/reaction/839902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPromethazine HydrochlorideHCID 6014—
ReactantDimethyl SulfateHCID 6497—
SolventAcetoneHCID 180—
ProductThiazinamium MetilsulfateHCID 6015—

Reaction Steps

dl-Promethazine hydrochloride (30 g.) was converted to the free base and was dissolved in absolute acetone and dimethyl sulfate (10 g.) was added (this is less than are equivalent of dimethyl sulfate due to its hazardous nature). After standing overnight, the solution was heated on a steam bath and cooled. The precipitated solid was filtered, washed with tetrahydrofuran and ether to provide dl-trimethyl[1-methyl-2-(phenothiazine-10-yl)ethyl]ammonium methyl sulfate, 27.6 g., m.p. 170°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04097596
Source datasetuspto-grants-1978_06
ORD IDord-bec2f61d3bcb4d9a9934737b21c253d8
Source noteuspto-grants-1978_06