Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659092Generated: October 25, 2026

Sodium hydride → 2-Dimethylsulphamoyl-7-fluoro-10-(3-(4-methylpiperazin-1-yl)propyl)phenothiazine

https://huagongshe.com/reaction/1659092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(3-Chloropropyl)-4-methylpiperazineHCID 66906—
ReactantN,N-dimethyl-7-fluoro-phenothiazine-2-sulphonamideHCID 21527012—
SolventDimethylformamideHCID 6228—
Product2-Dimethylsulphamoyl-7-fluoro-10-(3-(4-methylpiperazin-1-yl)propyl)phenothiazineHCID 2152701375.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03966930
Source datasetuspto-grants-1976_06
ORD IDord-0d47f33e0502409cb18c6acaab985618
Source noteuspto-grants-1976_06