HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-[10-[4-(1H-Imidazol-1-yl)phenoxy]decyl]-2-naphthalenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 10-[4-(1H-Imidazol-1-yl)phenoxy]decaneamine | HCID 54415265 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[10-[4-(1H-Imidazol-1-yl)phenoxy]decyl]-2-naphthalenesulfonamide | HCID 67598097 | — |
Reaction Steps
A suspension of 2.5 g of 10-[4-(1H-imidazol-1-yl)phenoxy]decaneamine (Example 66) in 250 ml of diethyl ether containing 3 ml of triethylamine is stirred while 2.0 g of 2-naphthalenesulfonylchloride is added. The reaction mixture is stirred at room temperature for 72 hours and 50 ml of H2O added. The solvents are decanted, leaving a viscous solid. The solid is dissolved in 100 ml of 50% aqueous ethanol. Careful concentration under a gentle stream of air gives a crystalline solid. The solid is collected washed with water and dried in vacuo at room temperature; m.p. 112°-115° C.; yield, 0.2 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05877196 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-2260ccf9c03040fc8ebfbf9f161255e8 |
| Source note | uspto-grants-1999_03 |