Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929373Generated: October 26, 2026

2-fluoro-N-methoxy-N,5-dimethylnicotinamide → Tert-butyl 4-(6-(2-fluoro-5-methylnicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/reaction/1929373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-fluoro-N-methoxy-N,5-dimethylnicotinamideHCID 57690476—
Reactanttert-Butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylateHCID 70700340—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(6-(2-fluoro-5-methylnicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylateHCID 5769050187%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of tert-butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylate (898 mg, 2.52 mmol) in tetrahydrofuran (10 ml) at −78° C. was added a 2.5M solution of nbutyllithium in hexanes (1.01 ml, 2.52 mmol) dropwise maintaining the temperature at −78° C. After complete addition, the solution was stirred at −78° C. for a further 20 minutes. A solution of 2-fluoro-N-methoxy-N,5-dimethylnicotinamide (500 mg, 2.52 mmol) in tetrahydrofuran (5 ml) was added dropwise at −78° C. and the reaction mixture was stirred at −78° C. for 1 hour. The reaction was quenched with a saturated solution of ammonium chloride. The mixture was stirred at room temperature for 20 minutes and extracted into ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography (ISCO Companion□, 40 g column, 0-20% EtOAc/Petrol) to afford the title compound as a sticky green oil (906 mg, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188071B2
Source datasetuspto-grants-2012_05
ORD IDord-5cfdfa8bc479410ba24d98435c04a36b
Source noteuspto-grants-2012_05