Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395314Generated: November 3, 2026

4-Acetylbenzenesulphonamide → HCID 18971518, compound

https://huagongshe.com/reaction/2395314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AcetylbenzenesulphonamideHCID 74065—
ReactantHCID 15524163HCID 15524163—
ProductHCID 18971518HCID 18971518—

Reaction Steps

As the starting substances, methyl 4-chloro-2-phenoxycarbonylaminobenzoate and 4-acetylbenzenesulfonamide were used and the same method was applied as in Example 36 to obtain N-(4-acetylbenzenesulfonyl)-N'-(2-methoxycarbonyl-5-chlorophenyl)urea and further to obtain from 300 mg (0.76 mmol) of N-(4-acetylbenzenesulfonyl)-N'-(2-carboxyl-5-chlorophenyl)urea 170 mg of the above-identified compound (yield 59.1%). Properties: colorless crystal, Melting point: >250° C. (decomposition), PMR (δppm, DMSO-d6):2.64 (3H,s), 7.10 (1H,s), 7.24 (1H,q), 7.85 (1H,d), 8.17 (2H,d), 8.27 (2H,d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814631
Source datasetuspto-grants-1998_09
ORD IDord-ce9abfbbf15049239cb24853c68d3c0f
Source noteuspto-grants-1998_09