HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2-Methylbutan-2-yl)benzene-1-sulfonyl chloride → n-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1,1-dimethyl-propyl)-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2-Methylbutan-2-yl)benzene-1-sulfonyl chloride | HCID 22281976 | — |
| Reactant | 4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenylamine | HCID 59428114 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | n-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1,1-dimethyl-propyl)-benzenesulfonamide | HCID 25135042 | — |
Reaction Steps
A 4 mL scintillation vial was charged with 4-chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenylamine (100 mg, 0.363 mmol), 4-(1,1-dimethyl-propyl)-benzenesulfonyl chloride (98 g, 0.399 mmol), and pyridine (1 mL). The resultant solution was stirred 4 hours at 80° C. and then partitioned with EtOAc/1 M HCl. The organics were subsequently washed with 1 M HCl, saturated aqueous sodium bicarbonate, and brine; dried over anhydrous sodium sulfate; and removed in vacuo. The resultant residue was then purified via automated silica gel chromatography to afford the desired sulfonamide: MS (ES) M+H expected 456.2, found 456.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409909B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-54dbdc7ba5a148b390f3d60e23dd47e7 |
| Source note | uspto-grants-2016_08 |