HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 86739979, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 54267812 | HCID 54267812 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86739979 | HCID 86739979 | — |
Reaction Steps
2.7 g of 1-methylpiperazine are added slowly to a suspension of 10.2 g of 5-[N-(1-adamantyl)-sulfamoyl]-isatoic anhydride in 250 ml of absolute toluene, at 100° with stirring. After the addition is ended, the mixture is stirred for a further 1 hour at 100° and is allowed to cool to room temperature, the precipitate is separated off by decanting and the crude product thus obtained is recrystallised from ethanol. 5-[N-(1-Adamantyl)-sulfamoyl]-anthranilic acid (4-methyl)-piperazide with a melting point of 214°-215° is obtained. (Melting point of the hydrochloride: 298°-300°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04505913 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-fe543b5ad57d481c88d3bbc31472b503 |
| Source note | uspto-grants-1985_03 |