HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 58974987, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(1H-Indol-3-yl)-2-(1-piperidinyl)ethanone | HCID 34864 | — |
| Reactant | 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride | HCID 58975125 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58974987 | HCID 58974987 | 57% |
Reaction Steps
Slowly add 1-(1H-Indol-3-yl)-2-piperidin-1-yl-ethanone (199 mg, 0.821 mmol, 1.0 eq) as a 2 ml DMF solution to a flask under N2 containing sodium hydride (36 mg, 60 wt % on oil, 0.903 mmol, 1.1 eq) in 2 ml DMF solution. Stir solution for 5 minutes. Slowly add 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (296 mg, 0.903 mmol, 1.1 eq) as a 3 ml DMF solution. Stir reaction for 18 hours at room temperature. Strip reaction of solvent and purify on silica gel chromatography to give N-(4-Fluoro-benzyl)-4-[3-(2-piperidin-1-yl-acetyl)-indole-1-sulfonyl]-benzamide (249 mg, 57% yield). Mass Spectrum (m/e): 534 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595339B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-a61c163ce6754524869ec62312a00324 |
| Source note | uspto-grants-2009_09 |