Hexylamine → HCID 15180169, compound
Reaction equation
Cl[C:2]1[C:3]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)=[N:4][S:5][N:6]=1.[CH2:13]([NH2:19])[CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]>CS(C)=O>[CH2:13]([NH:19][C:2]1[C:3]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)=[N:4][S:5][N:6]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine (0.59 g, 3 mmol) and hexylamine (1.52 g, 15 mmol) in DMSO (5 ml) was heated at 100° C. for 48 h. After evaporation, water was added to the residue and extracted with ether. The combined organic extract were dried and evaporated to give the title compound.
Workup
- customAfter evaporation, water
- additionwas added to the residue
- extractionextracted with ether
- extractionThe combined organic extract
- customwere dried
- customevaporated
Sources & evidence
- ORD record
- ord-189a9ef634234d8c860fd5ee8b5a34cc
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05712297
Reaction notes
Loading…