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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Chloroform tetrahydrofuran | HCID 21956068 | — |
| Reactant | 3,9-dimethyl-2-hydroxymethyl-9H-dibenzo [b,f]-imidazo[1,2-d][1,4]diazepine | HCID 53657903 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3,9-Dimethyl-2-[(4-methyl-1-piperazinyl)methyl]-9H-dibenz[b,f]imidazo[1,2-d][1,4]diazepine | HCID 21539214 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03956297 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-5510e451777049eca51dfd55023ae932 |
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| Source note | uspto-grants-1976_05 |
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