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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852023Generated: October 26, 2026

Potassium Fluoride → 3-{3-Cyano-6-[(2,2-dimethyl-propyl)-amino]-5-fluoro-pyridin-2-ylamino}-N-methoxy-4-methyl-benzamide

https://huagongshe.com/reaction/852023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant3-Amino-N-methoxy-4-methylbenzamideHCID 20767000—
Reactant2-Chloro-6-[(2,2-dimethyl-propyl)-amino]-5-fluoro-nicotinonitrileHCID 86588798—
SolventDimethyl SulfoxideHCID 679—
Product3-{3-Cyano-6-[(2,2-dimethyl-propyl)-amino]-5-fluoro-pyridin-2-ylamino}-N-methoxy-4-methyl-benzamideHCID 101346711%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 2-chloro-6-[(2,2-dimethyl-propyl)-amino]-5-fluoro-nicotinonitrile (150 mg, 0.62 mmol), 3-amino-N-methoxy-4-methyl-benzamide (150 mg, 0.83 mmol) and potassium fluoride (30 mg, 0.51 mmol) in DMSO (1 mL) was heated to 150° C. overnight. The reaction mixture was allowed to cool to room temp and then partitioned between water and ethyl acetate. The organic layer was dried (sodium sulfate) and concentrated under reduced pressure. The product (2.5 mg, 1%) was obtained after purification by silica gel chromatography with 30% EtOAc in hexane as eluent. C20H24FN5O2 MS m/e=386 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253174B2
Source datasetuspto-grants-2007_08
ORD IDord-d7d86ab8b68c46d4b050f45baeb8f0a4
Source noteuspto-grants-2007_08