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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714475Generated: November 1, 2026

Water → 4-({[6-amino-3,5-dicyano-4-(4-fluorophenyl)pyridin-2-yl]oxy}methyl)-N-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/714475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Amino-4-[4-fluorophenyl]-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrileHCID 11739479—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(hydroxymethyl)-N-methylpyridine-2-carboxamide hydrochloride hydrateHCID 66631382—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-({[6-amino-3,5-dicyano-4-(4-fluorophenyl)pyridin-2-yl]oxy}methyl)-N-methylpyridine-2-carboxamideHCID 66631060—

Reaction Conditions

Temperature60 °C

Reaction Steps

1.62 g (14.44 mmol) of potassium tert-butoxide were suspended in 10 ml of 1,2-dimethoxyethane. After addition of 1.44 g (8.66 mmol) of 4-(hydroxymethyl)-N-methylpyridine-2-carboxamide hydrochloride monohydrate (Example 40A) and 1.00 g (2.89 mmol) of 2-amino-4-[4-fluorophenyl]-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile (Example 38A), the mixture was stirred at 60° C. for 2 h and at RT overnight. 30 ml of water were added to the reaction mixture. The precipitate was filtered off and washed with water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187428B2
Source datasetuspto-grants-2015_11
ORD IDord-65e7bb050b2d4d8da5ff9215051d3197
Source noteuspto-grants-2015_11