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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 4-Methyl-10-(methylthio)-4H-thieno[3,4-b] [1,5]benzodiazepine | HCID 12521660 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methyl-10-(1-piperazinyl)-4H-thieno[3,4-b][1,5]benzodiazepine fumarate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04087421 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-e1d5247890034975b3d50245f834917e |
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| Source note | uspto-grants-1978_05 |
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