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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251716Generated: November 2, 2026

Sodium Dithionite → HCID 10167977, compound

https://huagongshe.com/reaction/2251716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
ReactantHCID 10211643HCID 10211643—
SolventEthanolHCID 702—
ProductHCID 10167977HCID 1016797720%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of N-[3,5-dibromo-4-(3-bromobenzyloxy)benzoyl]-4-nitrobenzenesulphonamide (0.25 mmol), prepared as described in Example 33, in ethanol (95%, 25 mL), sodium dithionite (1.26 mmol) was added and the reaction mixture stirred over night at 70° C. The reaction mixture was allowed to reach room temperature and then evaporated in vacuo. The residue was diluted with ethyl acetate and washed with an aqueous solution of sodium hydrogencarbonate (saturated). The organic phase was dried over magnesium sulphate and concentrated in vacuo. The residue was purified on column (silica gel, chloroform/methanol 17:3) and further purified by semi-preparative HPLC (column and eluents as described for Examples 27, 28 and 30) to give 30 mg (20%) of 4-amino-N-[3,5-dibromo-4-(3-bromobenzyloxy)-benzoyl]benzenesulphonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319163B2
Source datasetuspto-grants-2008_01
ORD IDord-682570e9b42344e7b25b28368867409d
Source noteuspto-grants-2008_01