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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-fluoro-N-methoxy-N,5-dimethylnicotinamide | HCID 57690476 | — |
| Reactant | tert-Butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylate | HCID 70700340 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(6-(2-fluoro-5-methylnicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylate | HCID 57690501 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08188071B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-5cfdfa8bc479410ba24d98435c04a36b |
|---|
| Source note | uspto-grants-2012_05 |
|---|