Thionyl Chloride → HCID 12333890, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([S:7]([NH:10][C:11]2[CH:19]=[CH:18][C:14]([C:15](O)=[O:16])=[CH:13][CH:12]=2)(=[O:9])=[O:8])[CH:2]=1.S(Cl)([Cl:22])=O>CN(C)C=O>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([S:7]([NH:10][C:11]2[CH:19]=[CH:18][C:14]([C:15]([Cl:22])=[O:16])=[CH:13][CH:12]=2)(=[O:9])=[O:8])[CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Into a 500 ml-flask fitted with a mechanical stirrer and a condenser were introduced 26 g (0.093 mol) of 4-(3-pyridylsulfonamido)-benzoic acid and 180 ml of thionyl chloride, after which a few drops of dimethylformamide were added as catalyst. The mixture was progressively heated to boiling, which was maintained for three hours.
Workup
- customInto a 500 ml-flask fitted with a mechanical stirrer and a condenser
- temperatureThe mixture was progressively heated to boiling, which
- temperaturewas maintained for three hours
Sources & evidence
- ORD record
- ord-3e063e87439a430f895aa42f34400f58
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04117151
Reaction notes
Loading…