Iodoethane → Tert-butyl 4-[(6-chloropyrazin-2-yl)(ethyl)amino]piperidine-1-carboxylate

To a stirred solution of tert-butyl 4-[(6-chloropyrazin-2-yl)amino]piperidine-1-carboxylate (0.20 g, 0.64 mmol) in tetrahydrofuran (3 mL) at −70° C. was added iodoethane (0.26 mL, 3.2 mmol) and NaHMDS (1M solution in THF; 1.3 mL, 1.3 mmol). The reaction mixture was warmed to room temperature. Iodoethane (0.26 mL, 3.2 mmol) and NaHMDS (1M solution in THF; 1.3 mL, 1.3 mmol) were added. The reaction mixture was stirred at 65° C. After 18 h, the reaction was quenched with saturated aqueous ammonium chloride (25 mL) and extracted with EtOAc (3×25 mL). The organic layers were combined, dried over magnesium sulfate, filtered and concentrated. The crude residue was purified by silica gel chromatography (EtOAc/Hexanes gradient) to afford tert-butyl 4-[(6-chloropyrazin-2-yl)(ethyl)amino]piperidine-1-carboxylate as a yellow solid. LRMS (ESI) calculated for C16H25ClN4O2 [M+Na]+, 363.2; found 363.1.

1. customthe reaction was quenched with saturated aqueous ammonium chloride (25 mL)
2. extractionextracted with EtOAc (3×25 mL)
3. dry with materialdried over magnesium sulfate
4. filtrationfiltered
5. concentrationconcentrated
6. customThe crude residue was purified by silica gel chromatography (EtOAc/Hexanes gradient)

ORD record

ord-6f10a685e15f4cddbaa645e940c98dc2

Source dataset

uspto-grants-2012_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08183245B2