HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3,4-Dihydroquinoline-1-carboxylic acid[6-(2-trifluoromethylbenzenesulfonylamino)-hexyl]amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-nitrophenyl 3,4-dihydroquinoline-1(2H)-carboxylate | HCID 17848819 | — |
| Reactant | n-(6-Aminohexyl)-2-trifluoromethylbenzene sulfonamide hydrochloride | HCID 22719673 | — |
| Product | 3,4-Dihydroquinoline-1-carboxylic acid[6-(2-trifluoromethylbenzenesulfonylamino)-hexyl]amide | HCID 22719672 | 61% |
Reaction Steps
To a solution of N-(6-Aminohexyl) -2-trifluoromethylbenzene sulfonamide Hydrochloride( 0.1 g, 0.27 mmol) dimethyl formamide (3 mL) and triethylamine (0.1 g, 1 mmol) was added 3, 4-Dihydro-2H-quinoline-1-carboxylic acid 4-nitrophenyl ester (0.09 g, 0.3 mmol) and the reaction mixture was stirred at room temperature for 4 h. Solvent was evaporated and purification by preparative TLC afford the titled compound as an oil (0.08 g, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211241B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-af5647c0ba424297b1e60868b4bb97b2 |
| Source note | uspto-grants-2001_04 |