HuagongsheHuagongshe Chemistry Print Report · For research reference only
Promethazine Hydrochloride → Thiazinamium Metilsulfate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Promethazine Hydrochloride | HCID 6014 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Thiazinamium Metilsulfate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04097596 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-bec2f61d3bcb4d9a9934737b21c253d8 |
| Source note | uspto-grants-1978_06 |