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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371648Generated: October 30, 2026

Piperazine → 4-Methyl-10-(1-piperazinyl)-4H-thieno[3,4-b][1,5]benzodiazepine fumarate

https://huagongshe.com/reaction/371648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantO-XyleneHCID 7237—
ReactantFumaric AcidHCID 444972—
Reactant4-Methyl-10-(methylthio)-4H-thieno[3,4-b] [1,5]benzodiazepineHCID 12521660—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product4-Methyl-10-(1-piperazinyl)-4H-thieno[3,4-b][1,5]benzodiazepine fumarateHCID 12521689—

Reaction Steps

A mixture comprising 2.6 g. of 4-methyl-10-(methylthio)-4H-thieno[3,4-b][1,5]benzodiazepine (U.S. Pat. No. 3,951,981 -- Ex. 7), 8.6 g. of piperazine, 3 drops of acetic acid and 15 ml. of xylene is stirred and refluxed for 4 hours. The reaction mixture is evaporated, washed with water and the residue is dissolved in 50 ml. of 2N acetic acid. The solution is filtered, the filtrate is made alkaline with ammonium hydroxide and extracted with benzene. The extracts are dried over magnesium sulfate, filtered and evaporated producing an amber oil. This oil is dissolved in 20 ml. of ethanol and a mixture of 2.1 g. of fumaric acid in 40 ml. of ethanol is added. The solid is collected and recrystallized from 125 ml. of methanol giving the desired product as the fumarate salt, m.p. 205°-206° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087421
Source datasetuspto-grants-1978_05
ORD IDord-e1d5247890034975b3d50245f834917e
Source noteuspto-grants-1978_05