HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 23355235, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 4,7-Dichloroquinoline | HCID 6866 | — |
| Reactant | 1-(2-Amino-1,1-dimethylethyl)piperidine | HCID 1713118 | — |
| Product | HCID 23355235 | HCID 23355235 | 31.6% |
Reaction Steps
4.57 g of 4,7-dichloroquinoline, 7.5 g of 2-methyl-2-(piperidin-1-yl)-propylamine and 0.75 g of phenol were reacted at 180° C. for 16 hours. The crude reaction product, isolated as in the preceeding Example, was purified on 200 g of aluminium oxide (activity grade II) prior to recrystallization; a 1:1 mixture of toluene and acetone was used as the eluent. After a fore-run, which contained unreacted 4,7-dichloroquinoline, the product was eluted and, after recrystallization from 5 ml of acetonitrile, yielded 0.8 g of colourless crystals, m.p.: 143°-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05596002 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-9a09b32cb1054981bb27fa8a71fade94 |
| Source note | uspto-grants-1997_01 |