HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691545Generated: October 27, 2026
Benzenesulfonyl chloride → HCID 57920397, compound
https://huagongshe.com/reaction/1691545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Benzo[b]thiophen-2-amine hydrochloride | HCID 66906726 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57920397 | HCID 57920397 | — |
Reaction Steps
Benzenesulfonyl chloride (0.661 mL, 5.15 mmol) was added to a solution of compound 1-C (0.87 g, 4.69 mmol) in pyridine (10 mL) at 0° C. The ice bath was removed and the solution was stirred at ambient temperature for 2 h. The solvent was evaporated in vacuo, and the residue was partitioned between 2 N HCl and dichloromethane. The organic layer was dried over magnesium sulfate and the solvent evaporated in vacuo. The residue was pre-absorbed on silica gel and purified by flash column chromatography, eluting with a gradient of ethyl acetate (10-50%) in heptane, to afford compound 1-D as a colorless solid (1.19 g, 88%). 1H-NMR (CDCl3): δ 6.96 (s, 1H), 7.25-7.34 (m, 2H), 7.44-7.49 (m, 2H), 7.55-7.66 (m, 3H), 7.84-7.88 (m, 2H); MS: m/z 290.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153682B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-17e19fa8c829490b911a56458ca7ef67 |
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| Source note | uspto-grants-2012_04 |
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