HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 4H-Thieno(3,4-b)(1,5)benzodiazepine, 10-(1-piperazinyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 12521659 | HCID 12521659 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4H-Thieno(3,4-b)(1,5)benzodiazepine, 10-(1-piperazinyl)- | HCID 3042388 | — |
Reaction Steps
A bomb charged with 2.5 g. of 10-(methylthio)-4H-thieno[3,4-b][1,5]benzodiazepine, 8.6 g. of piperazine, and three drops of acetic acid is placed in an oil bath and heated at 155°-160° C. for 4 days. The bomb is then cooled and the contents are dissolved in 2N acetic acid. The solution is filtered and the filtrate is made alkaline with ammonium hydroxide and extracted with chloroform. The extracts are dried, filtered and evaporated to give a yellow solid. Recrystallization from ethanol gives the product as light tan crystals which melt at 228°-231° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087421 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-cc6f6cc5ab9c4ef6986daf09cce11c4c |
| Source note | uspto-grants-1978_05 |