HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-[4-(3-nitro-7-phenylquinolin-4-ylamino)butyl]methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(4-aminobutyl)methanesulfonamide hydrochloride | HCID 21984197 | — |
| Reactant | 4-Chloro-3-nitro-7-phenylquinoline | HCID 21984335 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-[4-(3-nitro-7-phenylquinolin-4-ylamino)butyl]methanesulfonamide | HCID 21984203 | 82.7% |
Reaction Steps
N-(4-aminobutyl)methanesulfonamide hydrochloride (7.8 g, 39 mmol) was added to a suspension of 4-chloro-3-nitro-7-phenylquinoline (35 mmol) and triethylamine (8.0 g, 79 mmol) in NMP (80 mL), and the reaction was stirred at ambient temperature overnight. The resulting solution was poured into water (350 mL) to form a solid, which was isolated by filtration, washed with water, air-dried, and recrystallized from acetonitrile to provide 12.0 g of N-[4-(3-nitro-7-phenylquinolin-4-ylamino)butyl]methanesulfonamide as yellow plates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091214B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-8fccf99693c64fad9f96b1c8c8faeb9d |
| Source note | uspto-grants-2006_08 |