2-Aminopyridine → Tert-butyl 4-(imidazo[1,2-a]pyridin-3-yl)piperidine-1-carboxylate
Reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([CH:14](Br)[CH:15]=O)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[NH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=1>C(O)C>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[N:20]3[CH:21]=[CH:22][CH:23]=[CH:24][C:19]3=[N:18][CH:15]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]Participants
4
Procedure
To a solution of 1.15 g of 1-(t-butoxycarbonyl)-4-(1-bromo-2-oxoethyl)piperidine (from Procedure 23, Step C) in 15 mL ethanol was added 388 mg of 2-aminopyridine. After refluxing for 18 h, the solvent was evaporated. The mixture was partitioned between ethyl acetate and saturated sodium bicarbonate solution. Aqueous layer was extracted with ethyl acetate (3×). The combined organic phase was washed with brine, dried over magnesium sulfate and concentrated. The residue was purified by flash chromatography with 50% ethyl acetate in hexanes, followed by 100% ethyl acetate to give 401 mg of the title compound as a solid.
Workup
- temperatureAfter refluxing for 18 h
- customthe solvent was evaporated
- customThe mixture was partitioned between ethyl acetate and saturated sodium bicarbonate solution
- extractionAqueous layer was extracted with ethyl acetate (3×)
- washThe combined organic phase was washed with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customThe residue was purified by flash chromatography with 50% ethyl acetate in hexanes
Sources & evidence
- ORD record
- ord-0b2131bd87c24f83bb7b58b0234f95a8
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06432981B1
Reaction notes
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