HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1-(1-Benzenesulfonyl-2,3-dihydro-1H-indol-5-yl)-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(2,3-Dihydro-1H-indol-5-yl)ethan-1-one | HCID 253117 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(1-Benzenesulfonyl-2,3-dihydro-1H-indol-5-yl)-ethanone | HCID 14112956 | — |
Reaction Steps
1-(2,3-Dihydro-1H-indol-5-yl)-ethanone (0.200 g, 1.24 mmol) was dissolved in THF (2 ml) before pyridine (0.303 ml, 3.75 mmol) was added, leaving a yellow solution. The benzenesulfonyl chloride (0.220 g, 1.24 mmol) was then added, as a solid, with stirring. The reaction mixture was stirred at 40 C for 5 h. The mixture was cooled and the THF and pyridine were removed in vacuo. The desired sulfonamide (0.310 g, 1.02 mmol, 82%) was recrystallized from ethyl acetate and hexanes. It had LC-MS (ES+): 302 [MH]+ m/e
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07381749B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-1a284aaa23ec4f8f9029bbecc9b61d57 |
| Source note | uspto-grants-2008_06 |