HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705587Generated: October 30, 2026
Benzenesulfonyl chloride → HCID 57818855, compound
https://huagongshe.com/reaction/705587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | HCID 178474475 | HCID 178474475 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57818855 | HCID 57818855 | 49.6% |
Reaction Steps
N-(5-fluoro-2-hydroxypyrimidin-4-yl)-acetamide (200 mg, 1.17 mmol) was suspended in pyridine (5 mL) and stirred at ambient temperature. To the stirred suspension was added benzenesulfonyl chloride (226 mg, 1.29 mmol) and agitation was continued for 16 hours. The solvent was evaporated under a stream of nitrogen and the residue was suspended in dichloromethane (2-3 mL), placed directly onto a silica gel column, and eluted with ethyl acetate in petroleum ether (0-50% gradient) to isolate 180 mg, 0.58 mmol (49%) of the title compound as a white solid: mp 142-143° C.; 1H NMR (DMSO-d6) δ 10.96 (s, 1H), 8.67 (d, J=2.6 Hz, 1H), 8.12-8.06 (m, 2H), 7.86-7.79 (m, 1H), 7.73-7.65 (m, 2H), 2.98 (s, 3H); HPLC-MS (ESI) m/z 312 (M+H)+, 310 (M−H)−. *N-(5-fluoro-2-hydroxypyrimidin-4-yl)-acetamide can be prepared through known literature methods.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174970B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-6d23d5c3d3c54deea6e3aab771e73f58 |
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| Source note | uspto-grants-2015_11 |
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