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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371633Generated: October 30, 2026

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

https://huagongshe.com/reaction/371633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant4-Methyl-10-(methylthio)-4H-thieno[3,4-b] [1,5]benzodiazepineHCID 12521660—
CatalystAcetic AcidHCID 176—
SolventAcetic AcidHCID 176—
Product4-Methyl-10-(4-methyl-1-piperazinyl)-4H-thieno[3,4-b][1,5] benzodiazepineHCID 3057699—

Reaction Steps

A solution of 1.2 g. of 4-methyl-10-(methylthio)-4H-thieno[3,4-b][1,5]benzodiazepine in 6 ml. of N-methylpiperazine is treated with 2-3 drops of glacial acetic acid and heated under reflux for 4 days. The solution is concentratedto dryness and the residue is warmed with dilute acetic acid. The acidic solution is filtered, cooled, and made alkaline with concentrated ammonium hydroxide solution. The precipitate is collected, washed with water and dissolved in chloroform. The chloroform solution is dried and concentrated to an oil, which slowly crystallizes. Recrystallization from ethanol gives yellow crystals, m.p. 83°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087421
Source datasetuspto-grants-1978_05
ORD IDord-2b8e6549e1464b689285b0bd96501659
Source noteuspto-grants-1978_05