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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347347Generated: October 25, 2026

4-acetyl-N-methoxybenzenesulfonamide → HCID 11352666, compound

https://huagongshe.com/reaction/347347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-acetyl-N-methoxybenzenesulfonamideHCID 21082525—
Reactant2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehydeHCID 21981006—
ProductHCID 11352666HCID 1135266694%

Reaction Steps

The title compound was prepared in an analogous way as Ex-1 using 4-acetyl-N-methoxy-benzenesulfonamide (Ex-30A) and 2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehyde (Ex-15A), 94% yield, yellow solid, mp 214–216° C. 1H-NMR (300 MHz, CDCl3) δ 8.17 (d, J=16 Hz, 1H), 8.11 (d, J=8 Hz, 2H), 8.03 (d, J=8 Hz, 2H), 7.68 (s, 1H), 7.64 (d, J=7 Hz, 1H), 7.48 (d, J=16 Hz, 1H), 7.36 (d, J=8 Hz, 1H), 7.25–7.26 (m, 1H), 7.11–7.16 (m, 2H), 6.59 (s, 1H), 6.50 (s, 1H), 4.03 (s, 3H) 3.90 (s, 3H), 3.84 (s, 3H), 3.58 (s, 3H). MS m/z: 506 ([M]+, 30%), 476 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173129B2
Source datasetuspto-grants-2007_02
ORD IDord-50ebff60b5124c2fb050ff8c1b01a7a3
Source noteuspto-grants-2007_02