HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049423Generated: November 1, 2026
Water → N-(2'-fluoro-5'-methoxy-2-neopentyl-[1,1'-biphenyl]-4-yl)-2-nitrobenzenesulfonamide
https://huagongshe.com/reaction/1049423
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Reactant | 2'-Fluoro-5'-methoxy-2-neopentyl-[1,1'-biphenyl]-4-amine | HCID 117760031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2'-fluoro-5'-methoxy-2-neopentyl-[1,1'-biphenyl]-4-yl)-2-nitrobenzenesulfonamide | HCID 117759909 | 82.1% |
Reaction Steps
To a solution of 2′-fluoro-5′-methoxy-2-neopentyl-[1,1′-biphenyl]-4-amine (970 mg) in THF (34 mL) were added triethylamine (706 μL) and o-nitrobenzenesulfonyl chloride (823 mg) at 0° C., and the mixture was stirred at room temperature for 5 hr. Triethylamine (706 μL) and o-nitrobenzenesulfonyl chloride (374 mg) were further added at 0° C., and the mixture was stirred at room temperature for 20 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.31 g) as a yellow gummy substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09382188B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-01557cc45fd941efaacebdab65eb629e |
|---|
| Source note | uspto-grants-2016_07 |
|---|