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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469114Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 66973557, compound

https://huagongshe.com/reaction/1469114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 178484257HCID 178484257—
SolventPyridineHCID 1049—
ProductHCID 66973557HCID 6697355719%

Reaction Steps

To an 8 mL screw-cap vial were added pyridine (2 mL), N′-(5-fluoro-2-hydroxy-pyrimidin-4-yl)-N,N-dimethylformamidine (100 mg, 0.54 mmol), and benzenesulfonyl chloride (106 mg, 0.60 mmol), and the mixture was shaken at room temperature for 24 hours (h). The crude mixture was partitioned between ethyl acetate (EtOAc) and saturated aqueous sodium bicarbonate (satd aq NaHCO3), and the organic phase was dried over magnesium sulfate (MgSO4), filtered, and evaporated to yield 153 mg of crude material. Reverse phase chromatography furnished the title product as a white solid (33 mg, 19%): mp 203-204° C.; 1H NMR (300 MHz, CDCl3) δ 8.77 (s, 1H), 8.16-8.11 (m, 3H), 7.72-7.65 (m, 1H) 7.60-7.53 (m, 2H), 3.24 (s, 3H), 3.23 (s, 3H); ESIMS m/z 325 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006259B2
Source datasetuspto-grants-2015_04
ORD IDord-5f4f0f78b79c49edb2761d23b0d0b746
Source noteuspto-grants-2015_04