HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730206Generated: October 26, 2026
Benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amide → Benzo[b]thiophene-2-sulfonic acid
https://huagongshe.com/reaction/730206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amide | HCID 86240018 | — |
| Reactant | 2-Methoxy-5-(propane-2-sulfonyl)benzenesulfonyl chloride | HCID 86240025 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzo[b]thiophene-2-sulfonic acid | HCID 18176377 | 214.7% |
Reaction Steps
To a solution of benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)-amide (1 mmol) (prepared as in example 1) in DCM (2 mL) and pyridine (2 mL), 2-methoxy-5-(propane-2-sulfonyl)benzenesulfonyl chloride (1.1 mmol) was added at RT and the reaction mixture was then allowed to stir at RT overnight. The reaction mixture was then diluted with DCM (10 mL). The organic phase was washed with 10% aqueous HCl (10 mL), water (10 mL) and brine (10 mL). The organic phase was dried over anhydrous sodium sulfate, and concentrated under vacuum. The residue obtained was purified by flash column chromatography eluting with DCM/EtOAc to obtain 460 mg of benzo[b]thiophene-2-sulfonic acid {2-[2-methoxy-5-(propane-2 sulfonyl) benzenesulfonylamino]phenyl-amide. Tr 1.09 min; MS: 581.4 (M+1)+. 1H NMR (DMSO-d6, 400 MHz): δ 0.97 (d, 6H), 3.58 (m, 1H), 4.02 (s, 3H), 6.84 (dd, 1H), 7.96 (td, 1H), 7.10 (td, 1H), 7.23 (dd, 1H), 7.44-7.54 (m, 3H), 7.86 (d, 1H), 7.90 (s, 1H), 7.96 (d, 1H), 8.03 (dd, 2H), 9.22 (bs, 1H), 9.79 (s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582673B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-2c6e626166434788b43f5928cd7ee125 |
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| Source note | uspto-grants-2009_09 |
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