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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839293Generated: October 29, 2026

Potassium Hydroxide → 2-[2-(4-methyl-1-piperazinyl)ethylthio]-5-phenyl-7-chloro-3H-1,4-benzodiazepine difumarate

https://huagongshe.com/reaction/839293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantFumaric AcidHCID 444972—
ReactantThionordiazepamHCID 826706—
Reactant1-(2-Chloroethyl)-4-methylpiperazine dihydrochlorideHCID 11183940—
SolventEthanolHCID 702—
SolventSodium ChlorideHCID 5234—
SolventTetrahydrofuranHCID 8028—
Product2-[2-(4-methyl-1-piperazinyl)ethylthio]-5-phenyl-7-chloro-3H-1,4-benzodiazepine difumarateHCID 7062602151.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 5.7 g of 1,3-dihydro-5-phenyl-7-chloro-2H-1,4-benzodiazepine-2-thione in a solvent mixture comprising 57 ml of a 10% aqueous potassium hydroxide solution and 6 ml of tetrahydrofuran is added at room temperature with stirring 7.0 g of 1-chloro-2-(4-methyl-1-piperazinyl)ethane dihydrochloride, and the resulting mixture is stirred at 40° C. for 4 hours. The reaction mixture is diluted with an aqueous sodium chloride solution and then extracted with ethyl acetate. The extract is washed with water and dried over magnesium sulfate, and the solvent is removed by distillation under reduced pressure. An oily product obtained as the residue is dissolved in ethyl alcohol and added with 3.8 g of fumaric acid, and the solvent is distilled off under reduced pressure to obtain a crystalline product. Recrystallization from tetrahydrofuran to obtain 5.4 g of 2-[2-(4-methyl-1-piperazinyl)ethylthio]-5-phenyl-7-chloro-3H-1,4-benzodiazepine difumarate, m.p. 193°-194° C. (decomposition), yield 42%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04094870
Source datasetuspto-grants-1978_06
ORD IDord-bb0f7dfabc3d4a368241e4ef8a739ea5
Source noteuspto-grants-1978_06