1-Octanol → HCID 15180137, compound
Reaction equation
[Na].Cl[C:3]1[C:7]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)=[N:6][S:5][N:4]=1.[CH2:14]([OH:22])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]>>[CH2:14]([O:22][C:3]1[C:7]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)=[N:6][S:5][N:4]=1)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]Participants
4
Conditions
- Temperature
- 50 °C
Procedure
To a solution of sodium (350 mg, 15 mmol) in 1-octanol (10 ml) was added 3-(3-chloro-1,2,5-thiadiazol-4-yl)pyridine (590 mg, 3 mmol). The mixture was stirred at 50° C. for 1 h and evaporated. The residue was dissolved in water and extracted with methylene chloride. The combined organic phases were dried and evaporated to give the title compound.
Workup
- customevaporated
- dissolutionThe residue was dissolved in water
- extractionextracted with methylene chloride
- customThe combined organic phases were dried
- customevaporated
Sources & evidence
- ORD record
- ord-c887dffccc4b4fa7a5d9c16ed57df101
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05753683
Reaction notes
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