3-Pyridinesulfonamide,2-amino-(9CI) → 2H-Pyrido(2,3-e)-1,2,4-thiadiazine, 1,1-dioxide
Reaction equation
[NH2:1][C:2]1[C:7]([S:8]([NH2:11])(=[O:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[CH:12]([O-])([O-])OCC>>[S:8]1(=[O:9])(=[O:10])[C:7]2[CH:6]=[CH:5][CH:4]=[N:3][C:2]=2[NH:1][CH:12]=[N:11]1Participants
3
Procedure
A mixture of 2 g of 2-aminopyridine-3-sulfonamide (Preparation 6) and 20 cm3 of ethyl orthoformate is brought to reflux for 1 hour. After cooling, the crystalline precipitate obtained is collected on a filter and washed with ether.
Workup
- temperatureto reflux for 1 hour
- temperatureAfter cooling
- customthe crystalline precipitate obtained
- customis collected on
- filtrationa filter
- washwashed with ether
Sources & evidence
- ORD record
- ord-df4f45697ba344a8a960a60e28988795
- Source dataset
- uspto-grants-1995_10
- Patent number
- US05459138
Reaction notes
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