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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131109Generated: October 31, 2026

Thiomorpholine → 2-Chloro-4-(4-fluoro-2-methylphenyl)-6-(thiomorpholin-4-yl)pyridine-3-carbonitrile

https://huagongshe.com/reaction/131109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiomorpholineHCID 67164—
Reactant2,6-Dichloro-4-(4-fluoro-2-methylphenyl)pyridine-3-carbonitrileHCID 57355005—
SolventMethanolHCID 887—
Product2-Chloro-4-(4-fluoro-2-methylphenyl)-6-(thiomorpholin-4-yl)pyridine-3-carbonitrileHCID 5735500788.4%

Reaction Steps

Crude 3-cyano-2,6-dichloro-4-(4-fluoro-2-methylphenyl)pyridine, (32.44 g, 115.4 mmol) and 300 mL of methanol were added to a 500-mL, 3-necked flask (equipped with a 25-mL pressure-equilibrating addition funnel/dry N2 adapter, septum with teflon-coated thermocouple, and teflon paddle stirrer/glass shaft). Thiomorpholine (23.0 mL, 25.0 g, 242 mmol, 2.10 equiv) was added dropwise over a period of 22 minutes via the addition funnel, and the resulting mixture was stirred at 20–25° C. for 18 hours. The precipitate was filtered, washed with 30 mL of methanol, and dried to afford 35.47 g (88.4%) of 2-chloro-3-cyano-4-(4-fluoro-2-methylphenyl)-6-(thiomorpholino)pyridine as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384939B2
Source datasetuspto-grants-2008_06
ORD IDord-9c7910ea963f49559a4185eb16397f10
Source noteuspto-grants-2008_06