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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72664Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86276169, compound

https://huagongshe.com/reaction/72664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86276168HCID 86276168—
SolventPyridineHCID 1049—
ProductHCID 86276169HCID 862761695%

Reaction Steps

To a mixture of (E)-3-methoxy-6-((2,4,6-trimethoxystyrylsulfonyl)methyl)pyridin-2-amine (333 mg, 0.84 mmol) in dry pyridine (20 mL) cooling on an ice bath methanesulfonyl chloride (0.3 mL, 2 mmol) was added dropwise. The mixture was stirred at room temperature for 20 hours. After evaporated to dryness, the residue was purified by silica gel chromatography, eluting with PE/EtOAc (1:1 v/v) to afford 20 mg of the title compound as white powder. 1H-NMR (DMSO-d6): δ 3.26 (s, 3H, OCH3), 3.82 (s, 3H, CH3), 3.85 (s, 9H, 3×OCH3), 4.45 (s, 2H, CH2), 6.30 (s, 2H, Ph-H), 7.14 (d, 1H, J=15.6 Hz, CH), 7.15 (d, 1H, J=8.8 Hz, Py-H), 7.41 (d, 1H, J=8.4 Hz, Py-H), 7.56 (d, 1H, J=15.6 Hz, CH), 9.73 (s, 1H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829003B2
Source datasetuspto-grants-2014_09
ORD IDord-480af4abb772489f8a9797461de2bff3
Source noteuspto-grants-2014_09