HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499477Generated: October 29, 2026
Ethanesulfonyl chloride → HCID 59750102, compound
https://huagongshe.com/reaction/499477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-[6-(Aminomethyl)-2-pyridyl]-4h-1,3-benzothiazine-4-one trifluoroacetic acid salt | HCID 68458297 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59750102 | HCID 59750102 | 21.5% |
Reaction Steps
2-[6-(Aminomethyl)-2-pyridyl]-4H-1,3-benzothiazine-4-one trifluoroacetic acid salt (500 mg, 1.3 mmol) and ethanesulfonyl chloride (270 mg, 2.1 mmol) were dissolved in ethyl acetate (10 ml) and water (5 ml), and sodium hydrogen carbonate (270 mg, 3.2 mmol) was added thereto. The mixture was stirred at room temperature for 3 hrs. The reaction mixture was combined with ethyl acetate and water. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was subjected to a silica gel column chromatography. The fractions eluted with ethyl acetate-hexane (2:1, v/v) were collected, concentrated and recrystallized from hexane-tetrahydrofuran to give the titled compound (101 mg, 21%) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767665B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-edf8ed2614b34ccab0e8b43fff8de5f0 |
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| Source note | uspto-grants-2010_08 |
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