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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395313Generated: November 1, 2026

Sulfanilamide → Methyl 2-{[(4-aminobenzenesulfonylamino)carbonyl]amino}-4-chlorobenzoate

https://huagongshe.com/reaction/2395313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfanilamideHCID 5333—
ReactantHCID 15524163HCID 15524163—
ProductMethyl 2-{[(4-aminobenzenesulfonylamino)carbonyl]amino}-4-chlorobenzoateHCID 22347486—

Reaction Steps

As the starting substances, methyl 4-chloro-2-phenoxycarbonylaminobenzoate and 4-aminobenzenesulfonamide were used and the same method was applied as in Example 36 to obtain N-(4-aminobenzenesulfonyl)-N'-(2-methoxycarbonyl-5-chlorophenyl)urea and further to obtain from 470 mg (1.27 mmol) of N-(4-aminobenzenesulfonyl)-N'-(2-carboxy-5-chlorophenyl)urea 270 mg of the above-identified compound (yield 60.5%). Properties: colorless crystal, Melting point: >250° C. (decomposition), PMR (δppm, DMSO-d6):6.39 (2H,s), 6.63 (2H,d), 7.09 (1H,s), 7.22 (2H,d), 7.76 (2H,d), 7.83 (2H,d), 11.51 (1H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814631
Source datasetuspto-grants-1998_09
ORD IDord-1780a2bfb84042eb8d670796e8b1f1d1
Source noteuspto-grants-1998_09