1-Butanol → HCID 15180173, compound
Reaction equation
[Na].Cl[C:3]1[C:4]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)=[N:5][O:6][N:7]=1.[CH2:14]([OH:18])[CH2:15][CH2:16][CH3:17]>>[CH2:14]([O:18][C:3]1[C:4]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)=[N:5][O:6][N:7]=1)[CH2:15][CH2:16][CH3:17]Participants
4
Conditions
- Temperature
- 25 °C
Procedure
To a solution of sodium (150 mg, 6.5 mmol) in 1-butanol (5 ml) was added 3-(4-chloro-1,2,5-oxadiazol-3-yl)pyridine (350 mg, 1.9 mmol). The mixture was stirred at 25° C. for 2 h and evaporated. The residue was dissolved in water and extracted with ether. The combined organic phases were dried and evaporated to give the title compound.
Workup
- customevaporated
- dissolutionThe residue was dissolved in water
- extractionextracted with ether
- customThe combined organic phases were dried
- customevaporated
Sources & evidence
- ORD record
- ord-c3ea6b93a57d45a8833bc0b5933acd27
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05264444
Reaction notes
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