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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705587Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 57818855, compound

https://huagongshe.com/reaction/705587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 178474475HCID 178474475—
SolventPyridineHCID 1049—
ProductHCID 57818855HCID 5781885549.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174970B2
Source datasetuspto-grants-2015_11
ORD IDord-6d23d5c3d3c54deea6e3aab771e73f58
Source noteuspto-grants-2015_11