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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729637Generated: October 25, 2026

1-Butanol → N-[1-(3-cyano-4,6-dimethylpyridin-2-yl)azetidin-3-yl]-2-(3-fluorophenyl)pyrimidine-5-carboxamide

https://huagongshe.com/reaction/729637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantWaterHCID 962—
Reactant2-Chloro-4,6-dimethyl-3-pyridinecarbonitrileHCID 223261—
ReactantN-azetidin-3-yl-2-(3-fluorophenyl)pyrimidine-5-carboxamideHCID 57832989—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductN-[1-(3-cyano-4,6-dimethylpyridin-2-yl)azetidin-3-yl]-2-(3-fluorophenyl)pyrimidine-5-carboxamideHCID 6700655399.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a vial was added N-azetidin-3-yl-2-(3-fluorophenyl)pyrimidine-5-carboxamide (0.04 g, 0.13 mmol), 2-chloro-4,6-dimethylnicotinonitrile (32.5 mg, 0.19 mmol), and 0.3 mL each of n-butanol, TEA and water. The mixture was heated to 90° C. for 12 hrs and then diluted with ethyl acetate and brine. The layers were separated and the organic layer dried (Na2SO4) and the solvent removed to give a solid, which was purified by chromatography (silica, DCM to 1-5% MeOH/DCM) to give the product, N-[1-(3-cyano-4,6-dimethylpyridin-2-yl)azetidin-3-yl]-2-(3-fluorophenyl)pyrimidine-5-carboxamide (52 mg, 76%). HRMS (M+H)=403.1682 expected, 403.1750 observed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582643B2
Source datasetuspto-grants-2009_09
ORD IDord-43ddd8ea121c404d9d1c24c86271ab9f
Source noteuspto-grants-2009_09