HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6975Generated: October 25, 2026
p-Toluenesulfonic acid → N-[4-bromo-2-chlorobenzoyl]-5-bromothiophene-2-sulfonamide
https://huagongshe.com/reaction/6975
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Bromo-2-chlorobenzoic acid | HCID 108829 | — |
| Reactant | 5-Bromo-2-thiophenesulfonamide | HCID 1241304 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-bromo-2-chlorobenzoyl]-5-bromothiophene-2-sulfonamide | HCID 22019517 | — |
Reaction Steps
An 8 mL reaction vial is charged with 4-bromo-2-chlorobenzoic acid (0.39 mmol, 1.5 eq) and 2.0 mL of dichloromethane. A stock solution (4.0 mL) containing 5-bromothiophene-2-sulfonamide (0.26 mmol, 1 eq) and N,N-[dimethyl]-4-aminopyridine (48 mg, 0.39 mmol, 1.5 eq) in dichloromethane is added, followed by 0.261 g carbodiimide polystyrene resin (2.0 mmol/g, 0.52 mmol, 2.0 eq, Novabiochem) and the vial is capped and shaken. After 72 hr, 0.77 g sulphonated polystyrene resin (MP-TsOH) is added (1.53 mmol/g, 1.17 mmol, Argonaut). After about 18 hr the reaction mixture is filtered and concentrated under reduced pressure. Chromatography was applied to the residue and fractions containing product were combined and concentrated under reduce pressure to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084170B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-084376ff6cbd402bbcddd99c0de3c3d7 |
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| Source note | uspto-grants-2006_08 |
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