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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347357Generated: October 30, 2026

4-Acetylbenzenesulphonamide → 4-{3E-[5-(2-Aminophenylethynyl)-2,4-dimethoxyphenyl]acryloyl}benzenesulfonamide

https://huagongshe.com/reaction/347357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AcetylbenzenesulphonamideHCID 74065—
Reactant5-(2-Aminophenylethynyl)-2,4-dimethoxybenzaldehydeHCID 16115620—
Product4-{3E-[5-(2-Aminophenylethynyl)-2,4-dimethoxyphenyl]acryloyl}benzenesulfonamideHCID 6949031882.6%

Reaction Steps

Ex-35D: 4-{3E-[5-(2-Amino-phenylethynyl)-2,4-dimethoxyphenyl]acryloyl}benzenesulfonamide was prepared in a similar manner as Ex-1 using 4-acetylbenzenesulfonamide (Ex-35A) and 5-(2-amino-phenylethynyl)-2,4-dimethoxybenzaldehyde (Ex-35C), 82.6% yield, yellow solid, mp 167–169° C. 1H-NMR (300 MHz, DMSO-d6) δ 8.27 (d, J=8 Hz, 2H), 8.20(s, 1H), 8.01 (d, J=16Hz, 1H), 7.94 (d, J=8 Hz, 2H), 7.84 (d, J=16 Hz, 1H), 7.53 (s, 2H), 7.15–7.17 (m, 1H), 7.02–7.08 (m, 1H), 6.77 (s, 1H), 6.72 (d, J=8 Hz, 1H), 6.49–6.54 (m, 1H), 5.46 (br, 1H) 3.97 (s, 3H), 3.96 (s, 3H). MS m/z: 462 ([M+H]+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173129B2
Source datasetuspto-grants-2007_02
ORD IDord-4a5748c04700450ca3fcbbad48829b3d
Source noteuspto-grants-2007_02