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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435901Generated: October 30, 2026

Benzenesulfonamide, 4-amino-3,5-dichloro- → Methyl 2-{[(4-amino-3,5-dichlorobenzenesulfonylamino)carbonyl]amino}-4-chlorobenzoate

https://huagongshe.com/reaction/1435901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamide, 4-amino-3,5-dichloro-HCID 89607—
ReactantHCID 15524163HCID 15524163—
ProductMethyl 2-{[(4-amino-3,5-dichlorobenzenesulfonylamino)carbonyl]amino}-4-chlorobenzoateHCID 2234745145.4%

Reaction Steps

1.06 g (4.40 mmol) of 4-amino-3,5-dichloro-benzenesulfonamide and 1.34 g (4.40 mmol) of methyl 4-chloro-2-N-phenoxycarbonylanthranilate were treated in the same way as Preparation Example 1 to obtain 905 mg (yield 44%) of methyl 2-{[(4-amino-3,5-dichlorobenzenesulfonylamino)carbonyl]amino}-4-chlorobenzoate. Properties: colorless amorphous, PMR (δ ppm, DMSO-d6): 3.87 (3H, s), 6.59 (2H, br), 7.22 (1H, dd), 7.72 (2H, s), 7.93 (1H, d), 8.24 (1H, d), 10.17 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618977B2
Source datasetuspto-grants-2009_11
ORD IDord-d7d764c41d22498482a040b2a28af982
Source noteuspto-grants-2009_11