HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indoline → HCID 57565299, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indoline | HCID 10328 | — |
| Reactant | HCID 57565297 | HCID 57565297 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57565299 | HCID 57565299 | 75% |
Reaction Steps
5-|4-(4-Trifluoromethyl-phenyl)-piperazine-1-sulfonyl|-2,3-dihydro-1H-indole: 1-{5-[4-(4-Trifluoromethyl-phenyl)-piperazine-1-sulfonyl]-2,3-dihydro-indol-1-yl}-ethanone was refluxed in 1,4-dioxane (5 mL) and concentrate HCl (2.5 mL) for 2 h. The reaction was then diluted with dichloromethane and washed with 1N HCl, saturated sodium bicarbonate, dried (Na2SO4), filtered and concentrated to provide 5-[4-(4-trifluoromethyl-phenyl)-piperazine-1-sulfonyl]-2,3-dihydro-1H-indole (1.03 g, 75%) as an off-white solid. 1H NMR (400 MHz, CDCl3) δ 7.48-7.20(m, 4H) 6.88 (d, 2H), 6.60 (d, 1H), 3.70 (t, 2H), 3.36-3.33 (m, 4H), 3.15-3.12 (m, 4H), 3.10 (t, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517884B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-e95efeda7e8c4840a59ade74545adb3d |
| Source note | uspto-grants-2009_04 |