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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892288Generated: October 30, 2026

Sodium Dithionite → HCID 10167977, compound

https://huagongshe.com/reaction/892288

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 an 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 numberUS07005538B1
Source datasetuspto-grants-2006_02
ORD IDord-b2c0b67c86a147a8852aec5ce2258d32
Source noteuspto-grants-2006_02