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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264521Generated: October 30, 2026

3-Pyridinemethanol → 2-Amino-4-phenyl-6-(3-pyridinylmethoxy)-3,5-pyridinedicarbonitrile

https://huagongshe.com/reaction/2264521

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinemethanolHCID 7510—
Reactant2-amino-6-chloro-4-phenylpyridine-3,5-dicarbonitrileHCID 2786713—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystAcetic AcidHCID 176—
Product2-Amino-4-phenyl-6-(3-pyridinylmethoxy)-3,5-pyridinedicarbonitrileHCID 9858576—

Reaction Conditions

Temperature60 °C

Reaction Steps

102 mg (0.4 mmol) of 2-amino-6-chloro-4-phenyl-3,5-pyridinedicarbonitrile [Quintela et al., Heterocycles 38, 1299-1305 (1994)] and 54 mg (0.48 mmol) of potassium tert-butoxide are dissolved together in 1.696 g (=1.5 ml, 15.55 mmol) of 3-hydroxymethylpyridine, and the mixture is stirred at 60° C. for about 16 h. The resulting suspension is acidified with two drops of glacial acetic acid. The product which crystallizes out is filtered off with suction, washed with water and dried under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855219B2
Source datasetuspto-grants-2010_12
ORD IDord-705059d9258246a0b96d89126759683b
Source noteuspto-grants-2010_12