HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dimethylpiperidine → 2,7-bis(3,5-dimethylpiperidin-1-ylsulfonyl)-10-methylacridin-9(10H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dimethylpiperidine | HCID 118259 | — |
| Reactant | HCID 59355212 | HCID 59355212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,7-bis(3,5-dimethylpiperidin-1-ylsulfonyl)-10-methylacridin-9(10H)-one | HCID 46851181 | — |
Reaction Steps
To a solution of 10-methyl-9-oxo-9,10-dihydroacridine-2,7-disulfonyl dichloride from Example 7 (810 mg, 2 mmole) in THF (20 mL) was added 3,5-dimethylpiperidine (2 mL, 15 mmole) and the reaction mixture was stirred at room temperature for 6 hours. Solvent was evaporated and the residue was treated with 1 N HCl (50 mL) and stirred for 10 minutes. Yellow product was collected by filtration, washed with water and methanol and dried. Crude material was crystallized from chloroform-ethanol to provide 900 mg (80%) of yellow 11-4. MS 560 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120754B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-0ae59f7f6f4c4475ac094b14db351635 |
| Source note | uspto-grants-2015_09 |