HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892288Generated: October 30, 2026
Sodium Dithionite → HCID 10167977, compound
https://huagongshe.com/reaction/892288
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | HCID 10211643 | HCID 10211643 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10167977 | HCID 10167977 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005538B1 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-b2c0b67c86a147a8852aec5ce2258d32 |
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| Source note | uspto-grants-2006_02 |
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