Potassium Carbonate → 4-Ethyl-5-ethynylpyridin-2-amine
Reaction equation
[CH2:1]([C:3]1[C:8]([C:9]#[C:10][Si](C)(C)C)=[CH:7][N:6]=[C:5]([NH2:15])[CH:4]=1)[CH3:2].C([O-])([O-])=O.[K+].[K+]>CO>[CH2:1]([C:3]1[C:8]([C:9]#[CH:10])=[CH:7][N:6]=[C:5]([NH2:15])[CH:4]=1)[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is synthesized according to general procedure GP3 starting from 3.3 g (15 mmol) 4-ethyl-5-trimethylsilanylethynyl-pyridin-2-ylamine and 1.04 g (7.5 mmol) K2CO3 in 30 mL MeOH. The product is purified by chromatography on silica gel using a DCM/MeOH gradient. Yield: 1.78 g (81%).
Workup
- customThe product is purified by chromatography on silica gel using a DCM/MeOH gradient
Sources & evidence
- ORD record
- ord-b78c03d699024a24936a26f0a2956554
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618111B2
Reaction notes
Loading…