Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347363Generated: October 26, 2026

4-acetyl-N-(5-methylisoxazole-3-yl)benzenesulfonamide → 4-[3E-(2,4-Dimethoxy-5-pyrrolidin-1-yl-phenyl)acryloyl]-N-(5-methyl-isoxazol-3-yl)benzenesulfonamide

https://huagongshe.com/reaction/347363

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-acetyl-N-(5-methylisoxazole-3-yl)benzenesulfonamideHCID 8519026—
Reactant2,4-Dimethoxy-5-pyrrolidin-1-ylbenzaldehydeHCID 21082510—
Product4-[3E-(2,4-Dimethoxy-5-pyrrolidin-1-yl-phenyl)acryloyl]-N-(5-methyl-isoxazol-3-yl)benzenesulfonamideHCID 58800225—

Reaction Steps

The title compound was prepared in a similar manner as Ex-1 using 4-acetyl-N-(5-methyl-isoxazol-3-yl)benzenesulfonamide (Ex-1B, 0.30 g, 1.07 mmol) and 2,4-dimethoxy-5-pyrrolidin-1-ylbenzaldehyde (Ex-38B, 0.25 g, 1.07 mmol) as a dark red solid, mp 164–165° C. 1H-NMR (300 MHz, CDCl3) δ 8.09–7.93 (m, 4H), 7.35 (d, J=15.3 Hz, 1H), 7.05 (s, 1H), 6.48 (s, 1H), 6.24 (s, 1H), 3.92 (s, 3H), 3.90 (s, 3H), 3.29–3.18 (m, 4H), 2.38 (s, 3H), 2.02–1.91 (s, 4H). MS m/z: 498 (M+), 100%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173129B2
Source datasetuspto-grants-2007_02
ORD IDord-4132ac1ffa1a4bd4a7c8224d7fbbb86a
Source noteuspto-grants-2007_02