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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076213Generated: October 26, 2026

Methanesulfonyl chloride → 3,9-Dimethyl-2-[(4-methyl-1-piperazinyl)methyl]-9H-dibenz[b,f]imidazo[1,2-d][1,4]diazepine

https://huagongshe.com/reaction/1076213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-MethylpiperazineHCID 53167—
ReactantChloroform tetrahydrofuranHCID 21956068—
Reactant3,9-dimethyl-2-hydroxymethyl-9H-dibenzo [b,f]-imidazo[1,2-d][1,4]diazepineHCID 53657903—
SolventTriethylamineHCID 8471—
Product3,9-Dimethyl-2-[(4-methyl-1-piperazinyl)methyl]-9H-dibenz[b,f]imidazo[1,2-d][1,4]diazepineHCID 21539214—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A sampmle of 3,9-dimethyl-2-hydroxymethyl-9H-dibenzo[b,f]-imidazo[1,2-d] [1,4]diazepine is suspended in a chloroform/tetrahydrofuran mixture and treated with triethylamine. After cooling to -20° C. methanesulfonyl chloride is added with stirring at -20° C. The mixture is treated with 4-methylpiperazine and warmed gradually to room temperature. Work-up from an aqueous base followed by the usal purification techniques affords the product 3,9-dimethyl-2-(4-methyl-1-piperazinyl)methyl-9H-dibenz[b,f]-imidazo[1,2-d][1,4]diazepine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03956297
Source datasetuspto-grants-1976_05
ORD IDord-5510e451777049eca51dfd55023ae932
Source noteuspto-grants-1976_05