HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 2-Dimethylsulphamoyl-7-fluoro-10-(3-(4-methylpiperazin-1-yl)propyl)phenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(3-Chloropropyl)-4-methylpiperazine | HCID 66906 | — |
| Reactant | N,N-dimethyl-7-fluoro-phenothiazine-2-sulphonamide | HCID 21527012 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Dimethylsulphamoyl-7-fluoro-10-(3-(4-methylpiperazin-1-yl)propyl)phenothiazine | HCID 21527013 | 75.6% |
Reaction Steps
12 grams of N,N-dimethyl-7-fluoro-phenothiazine-2-sulphonamide were dissolved in 50 milliliters of dry dimethylformamide, 1.9 grams of 50% sodium hydride in oil added and the mixture stirred for 1 hour. 7.2 grams of 1-(3-chloropropyl)-4-methylpiperazine were then added and the mixture heated for two hours on a steam bath. Then the mixture was poured onto crushed ice, the resulting mixture extracted with ether, the ether phase washed, dried over anhydrous magnesium sulphate and the ether evaporated. 13 grams of 2-dimethylsulphamoyl-7-fluoro-10-(3-(4-methylpiperazin-1-yl)propyl)phenothiazine was thus obtained as a yellow oil. The dimaleate was made from an ethanol solution of the base and melted at 166°-169° Centigrade.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03966930 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-0d47f33e0502409cb18c6acaab985618 |
| Source note | uspto-grants-1976_06 |