HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191312Generated: November 2, 2026
Benzenesulfonyl chloride → HCID 56651012, compound
https://huagongshe.com/reaction/1191312
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | HCID 56651011 | HCID 56651011 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 56651012 | HCID 56651012 | 15% |
Reaction Steps
To a solution of 4-(3-aminophenyl)-1H-benzo[h]quinazolin-2-one (20 mg, 0.07 mmol) in pyridine (3 mL) was added benzenesulfonyl chloride (127 μL, 0.99 mmol), and stirred at 80° C. for 5 hours. After the solution was cooled to room temperature, the solvent was removed under reduced pressure. The residue was diluted with chloroform, washed with a saturated aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, the residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1), to give the titled compound as a yellow amorphous form (5 mg, yield 15%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680110B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-84e424c42257476e9b146949df322e8c |
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| Source note | uspto-grants-2014_03 |
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