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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838973Generated: November 1, 2026

2-Aminobenzenesulfonamide → 3-(2-Aminobenzenesulfonyl)-7-Chloro-2,4(1H,3H)-Quinazolinedione

https://huagongshe.com/reaction/1838973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzenesulfonamideHCID 72894—
ReactantHCID 15524163HCID 15524163—
Product3-(2-Aminobenzenesulfonyl)-7-Chloro-2,4(1H,3H)-QuinazolinedioneHCID 984139258%

Reaction Steps

2.7 g (15.7 mmol) of 2-aminobenzenesulfonamide and 4.8 g (15.7 mmol) of methyl 4-chloro-2-N-phenoxycarbonylanthranilate were treated in the same way as Preparation Example 1 to obtain 3.2 g (yield 58%: 3 steps) of the above-identified compound. Properties: colorless crystal, Melting point: >200° C. (decomposition), PMR (δ ppm, DMSO-d6): 6.46 (2H, s), 6.65 (1H, t), 6.81 (1H, d), 7.12 (1H, s), 7.23 (1H, d), 7.34 (1H, t), 7.76 (1H, d), 7.86 (1H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677344B2
Source datasetuspto-grants-2004_01
ORD IDord-472835a50e464fed987a1523725b2ce7
Source noteuspto-grants-2004_01