Ammonia → 3-Methoxy-2,7-naphthyridine
Reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[C:9]([C:11]#[C:12][Si](C)(C)C)[C:6]([CH:7]=O)=[CH:5][N:4]=1.[NH3:17]>CO>[CH3:1][O:2][C:3]1[N:4]=[CH:5][C:6]2[C:9]([CH:10]=1)=[CH:11][CH:12]=[N:17][CH:7]=2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6-Methoxy-4-[(trimethylsilyl)ethynyl]nicotinaldehyde (0.25 g, 1.1 mmol) and 7M ammonia in MeOH (5 mL) were stirred in a sealed vial at 80° C. overnight. The solution was concentrated, taken up in saturated sodium carbonate and extracted with ether. The organic phase was dried, filtered and concentrated to give 0.20 g of the title product.
Workup
- concentrationThe solution was concentrated
- extractionextracted with ether
- customThe organic phase was dried
- filtrationfiltered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-4cc53a28afca4c0490242e58570f34b0
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07700604B2
Reaction notes
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