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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347387Generated: October 29, 2026

5-(1H-indol-2-yl)-2,4-dimethoxybenzaldehyde → 4-{3E-[5-(1H-Indol-2-yl)-2,4-dimethoxyphenyl]acryloyl}-N-pyridin-2-ylbenzenesulfonamide

https://huagongshe.com/reaction/347387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(1H-indol-2-yl)-2,4-dimethoxybenzaldehydeHCID 16115621—
Reactant5-(1-acetyl-1H-indol-2-yl)-2,4-dimethoxybenzaldehydeHCID 21082530—
Reactant4-Acetyl-N-(2-pyridyl)benzenesulfonamideHCID 22750327—
Product4-{3E-[5-(1H-Indol-2-yl)-2,4-dimethoxyphenyl]acryloyl}-N-pyridin-2-ylbenzenesulfonamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173129B2
Source datasetuspto-grants-2007_02
ORD IDord-278ea6195e5c4f0e9b60dd8cba55d90c
Source noteuspto-grants-2007_02