HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2-Phenyl-azetidin-1-yl)-[4-(3-phenyl-indole-1-sulfonyl)-phenyl]-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium | HCID 124335 | — |
| Reactant | 2-Phenylazetidine | HCID 568971 | — |
| Reactant | 4-(3-Phenyl-indole-1-sulfonyl)-benzoic acid | HCID 58975141 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Phenyl-azetidin-1-yl)-[4-(3-phenyl-indole-1-sulfonyl)-phenyl]-methanone | HCID 58975047 | 92% |
Reaction Steps
Combine 4-(3-phenyl-indole-1-sulfonyl)-benzoic acid (125 mg, 0.33 mmol) and 2-phenyl-azetidine (100 mg, 0.75 mmol, excess) in dichloromethane (1.0 mL) and triethylamine (0.300 mL, 2.15 mmol, excess) and add benzotriazol-1-yloxytris(dimethylamino)phosphonium hexfluorophosphate (BOP Reagent) (150 mg, 0.33 mmol) at room temperature. Stir for 30 minutes, load entire reaction directly onto pre-packed silica gel column and purify by flash column chromatography (EtOAc/Hexanes) to yield 149 mg of (2-Phenyl-azetidin-1-yl)-[4-(3-phenyl-indole-1-sulfonyl)-phenyl]-methanone as a glassy solid (92%). LRMS: MH+ 493.08.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276516B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-5f9d4de2a4e94fcc93eaa0598e77d49d |
| Source note | uspto-grants-2007_10 |