HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730207Generated: October 26, 2026
Methyl 3-(chlorosulfonyl)-4-methoxybenzoate → 3-[2-(Benzo[b]thiophene-2-sulfonylamino)phenylsulfamoyl]-4-methoxybenzoic acid methyl ester
https://huagongshe.com/reaction/730207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3-(chlorosulfonyl)-4-methoxybenzoate | HCID 2794613 | — |
| Reactant | Benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amide | HCID 86240018 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[2-(Benzo[b]thiophene-2-sulfonylamino)phenylsulfamoyl]-4-methoxybenzoic acid methyl ester | HCID 11685190 | 65.7% |
Reaction Steps
To a solution of benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)-amide (1 mmol) in DCM (2 mL) and pyridine (2 mL), methyl 3-(chlorosulfonyl)-4-methoxybenzoate (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 350 mg of 3-[2-(benzo[b]thiophene-2-sulfonylamino)phenylsulfamoyl]-4-methoxybenzoic acid methyl ester. Tr 1.10 min, MS: 533.7 (M+1)+. 1H NMR (CDCl3, 400 MHz): δ 3.84 (s, 3H), 4.18 (s, 3H), 7.0-7.2 (m, 5H), 7.4-7.6 (m, 3H), 7.66 (s, 1H), 7.80 (d, 1H), 7.83 (d, 1H), 8.22 (dd, 1H), 8.34 (d, 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-489cef9e3c8142ecbab82c1b31076875 |
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| Source note | uspto-grants-2009_09 |
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