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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884196Generated: October 30, 2026

2-Aminobenzenesulfonamide → 2-Amino-5-iodobenzenesulfonamide

https://huagongshe.com/reaction/884196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzenesulfonamideHCID 72894—
ReactantN-IodosuccinimideHCID 120273—
Product2-Amino-5-iodobenzenesulfonamideHCID 22324088—

Reaction Steps

Commercially available 2-aminobenzenesulfonamide can be treated with N-iodosuccinimide (NIS) to afford 2-amino-5-iodo-benzenesulfonamide. Acylation with a malonyl halide monoester, such as ethyl 3-chloro-3-oxo-propionate, or with a dialkyl malonate, such as diethyl malonate, affords the corresponding amide, which can simultaneously be cyclized to the thiadiazine-dioxide and hydrolyzed to the desired acid intermediate (or a salt thereof, e.g., sodium salt).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236948B2
Source datasetuspto-grants-2012_08
ORD IDord-fc804453b2ba45eda65a523f27721e73
Source noteuspto-grants-2012_08