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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283334Generated: October 31, 2026

P-Toluenesulfonylhydrazide → 5-Chloro-2-(2-(4-chloro-2-methoxyphenyl)ethylsulfonamido)benzenesulfonamide

https://huagongshe.com/reaction/2283334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ToluenesulfonylhydrazideHCID 15303—
ReactantSodium AcetateHCID 517045—
Reactant(E)-5-chloro-2-(2-(4-chloro-2-methoxyphenyl)vinylsulfonamido)benzenesulfonamideHCID 57751036—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-2-(2-(4-chloro-2-methoxyphenyl)ethylsulfonamido)benzenesulfonamideHCID 5775096144.3%

Reaction Conditions

Temperature180 °C

Reaction Steps

Sodium acetate (64 mg, 0.78 mmol) and para-toluenesulfonhydrazide (145 mg, 0.78 mmol) was added to a solution of (E)-5-chloro-2-(2-(4-chloro-2-methoxyphenyl)vinylsulfonamido)benzenesulfonamide (85 mg, 0.19 mmol) in tetrahydrofuran (3 mL). The reaction mixture was heated at 180° C. for 15 min in a microwave reactor. The solids were removed by filtration, washed with tetrahydrofuran and the combined filtrates were evaporated. Purification by preparative HPLC gave 0.037 g (43% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-fc816705ef4d4e9db6e79c8753557056
Source noteuspto-grants-2015_09