HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-[4-(6-Chloropyrazin-2-yl)piperazin-1-yl]butan-1-amine → 5,5a,8,8a-Tetrahydro-3-[4-[4-(6-chloro-2-pyrazinyl)-1-piperazinyl]butyl]-1,5-methanocyclopent[d]azepine-2,4(1H,3H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-[4-(6-Chloropyrazin-2-yl)piperazin-1-yl]butan-1-amine | HCID 14086526 | — |
| Reactant | Bicyclo[3.3.0]oct-6-ene-2,4-dicarboxylic anhydride | HCID 53699477 | — |
| Product | 5,5a,8,8a-Tetrahydro-3-[4-[4-(6-chloro-2-pyrazinyl)-1-piperazinyl]butyl]-1,5-methanocyclopent[d]azepine-2,4(1H,3H)-dione | HCID 14370166 | — |
Reaction Steps
The title compound was prepared from 2.1 g (12 mmoles) of bicyclo[3.3.0]oct-6-ene-2,4-dicarboxylic anhydride and 3.2 g (12 mmoles) of 1-(4-aminobutyl)-4-(6-chloro-2-pyrazinyl)piperazine following the procedure in Example 4. 620 mg of the hydrochloride salt was isolated as the hemihydrate, m.p. 222°-224° C., after two recrystallizations from isopropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824999 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-5fd8d84f1d2d498a840a10b1e167bcc0 |
| Source note | uspto-grants-1989_04 |