HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 4-Methyl-10-(4-methyl-1-piperazinyl)-4H-thieno[3,4-b][1,5] benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 4-Methyl-10-(methylthio)-4H-thieno[3,4-b] [1,5]benzodiazepine | HCID 12521660 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Methyl-10-(4-methyl-1-piperazinyl)-4H-thieno[3,4-b][1,5] benzodiazepine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087421 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-2b8e6549e1464b689285b0bd96501659 |
| Source note | uspto-grants-1978_05 |