HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylhomopiperazine → HCID 13175261, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylhomopiperazine | HCID 228349 | — |
| Reactant | HCID 11148455 | HCID 11148455 | — |
| Product | HCID 13175261 | HCID 13175261 | — |
Reaction Steps
A mixture was prepared from 5.0 g of 2-chloro-6,7,8,9-tetrahydropyridazino[1,6-a]benzimidazole and 30 ml of 1-methylhomopiperazine and this was stirred and heated at reflux for 18 hours. The reaction mixture was then cooled and excess amine was removed by distillation to leave a tan solid residue. This solid was partitioned between methylene chloride and an aqueous 1% solution of sodium hydroxide. The methylene chloride layer was separated and the solvent was evaporated under reduced pressure to leave a residual solid. This solid was recrystallized from a mixture of ethanol and water to give 2-(4-methyl-1-homopiperazinyl)-6,7,8,9-tetrahydropyridazino[1,6-a]benzimidazole melting at about 106°-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04391806 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-1ac25303ee6e487fb5b29f85bda7ad7c |
| Source note | uspto-grants-1983_07 |