HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(1H-indol-2-yl)-2,4-dimethoxybenzaldehyde → 4-{3E-[5-(1H-Indol-2-yl)-2,4-dimethoxyphenyl]acryloyl}-N-pyridin-2-ylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(1H-indol-2-yl)-2,4-dimethoxybenzaldehyde | HCID 16115621 | — |
| Reactant | 5-(1-acetyl-1H-indol-2-yl)-2,4-dimethoxybenzaldehyde | HCID 21082530 | — |
| Reactant | 4-Acetyl-N-(2-pyridyl)benzenesulfonamide | HCID 22750327 | — |
| Product | 4-{3E-[5-(1H-Indol-2-yl)-2,4-dimethoxyphenyl]acryloyl}-N-pyridin-2-ylbenzenesulfonamide | HCID 11238019 | — |
Reaction Steps
NH4Cl (25 mL) and transferred to a separatory funnel containing THF (50 mL), EtOAc (50 mL) and H2O (50 mL). The layers were cut and the organic layer was concentrated to dryness. The crude product was suspended in EtOH (50 mL), filtered and then dried under vacuum to afford 2.5 g (85% yield) of the title compound, analytical dada identical as above. Similarly, the title compound could be prepared from 4-acetyl-N-pyridin-2-ylbenzenesulfonamide (Ex-5A) and 5-(1-acetyl-1H-indol-2-yl)-2,4-dimethoxybenzaldehyde (Ex-57F) or 5-(1H-indol-2-yl)-2,4-dimethoxybenzaldehyde (Ex-57D or Ex-57DD).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173129B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-278ea6195e5c4f0e9b60dd8cba55d90c |
| Source note | uspto-grants-2007_02 |