HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57158Generated: October 30, 2026
Benzenesulfonyl chloride → HCID 66908232, compound
https://huagongshe.com/reaction/57158
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Thieno[3,2-b]pyridin-2-ylamine hydrochloride | HCID 66907303 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 66908232 | HCID 66908232 | 25.2% |
Reaction Steps
To a suspension of compound 146-A (0.65 g, 2.91 mmol) in pyridine (30 mL), at rt, was added benzenesulfonyl chloride (0.751 mL, 5.83 mmol), and the reaction was stirred for 16 h. Additional benzenesulfonyl chloride (0.225 mL, 1.76 mmol) was added and the reaction mixture was stirred at rt for an additional 16 h. The solvent was evaporated in vacuo, the residue treated with 1N HCl and extracted several times with dichloromethane and ethyl acetate. The aqueous layer was filtered, dissolved in methanol, and the combined organic extracts were evaporated in vacuo. The resultant residue was purified by reverse phase HPLC, eluting with an MeCN—H2O gradient to afford compound 146-B as an orange solid (0.24 g, 20%). 1H-NMR (CD3CN): δ 6.92 (s, 1H), 7.2 8.0 (d of d, 1H), 7.46 (m, 2H), 7.56 (m, 1H), 7.85 (m, 2H), 8.27 (d, 1H), 8.35 (d, 1H); MS: m/z 291.09 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434711B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-8b5233d2c48c40f2b90229c4a4fffe68 |
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| Source note | uspto-grants-2016_09 |
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