HCID 15651240, compound → HCID 178456991, compound
Reaction equation
CS[C:3]1[NH:8][C:7]2[CH:9]=[CH:10][N:11]=[CH:12][C:6]=2[S:5](=[O:14])(=[O:13])[N:4]=1>C(N)(C)C>[CH:7]([NH:8][C:3]1[NH:8][C:7]2[CH:9]=[CH:10][N:11]=[CH:12][C:6]=2[S:5](=[O:14])(=[O:13])[N:4]=1)([CH3:9])[CH3:6]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 0.7 g of 3-methylthio-4H-pyrido[4,3-e][1,2,4]thiadiazine 1,1-dioxide obtained in Example 39 in 7 cm3 of isopropylamine is maintained in a sealed tube at 150° C. for 4 hours. After cooling, the solution is concentrated to dryness, the residue is taken up in 10 cm3 of water and the pH is adjusted to the value of 7. The precipitate obtained is collected on a filter, washed with water and recrystallized from hot water.
Workup
- temperatureAfter cooling
- concentrationthe solution is concentrated to dryness
- customThe precipitate obtained
- customis collected on a filter
- washwashed with water
- customrecrystallized from hot water
Sources & evidence
- ORD record
- ord-0a1c5dcb70934921885b59248b2a4019
- Source dataset
- uspto-grants-1995_10
- Patent number
- US05459138
Reaction notes
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