Sulfuric Acid → HCID 12562796, compound
Reaction equation
[Cl:1][C:2]1[N:3]=[N:4][C:5]([N:8]2[C:12]([NH2:13])=[C:11]([C:14]#[N:15])[CH:10]=[N:9]2)=[CH:6][CH:7]=1.S(=O)(=O)(O)[OH:17]>>[Cl:1][C:2]1[N:3]=[N:4][C:5]([N:8]2[C:12]([NH2:13])=[C:11]([C:14](=[O:17])[NH2:15])[CH:10]=[N:9]2)=[CH:6][CH:7]=1Participants
3
Procedure
A mixture of 3 g. of 3-chloro-6-(4-cyano-5-amino-1-pyrazolyl)-pyridazine (prepared according to Example 24) and 10.5 ml. of concentrated sulphuric acid is stirred at room temperature for one hour. Then the mixture is poured onto ice, the precipitate filtered, washed with water and triturated with 15 ml. of hot ethanol, filtered and dried. Yield: 3.05 g. (93.5%); m.p.: 314°-317° C.
Workup
- additionA mixture of 3 g
- additionThen the mixture is poured onto ice
- filtrationthe precipitate filtered
- washwashed with water
- customtriturated with 15 ml
- filtrationof hot ethanol, filtered
- customdried
Sources & evidence
- ORD record
- ord-dc99a3182f41456c85b997894c2233ed
- Source dataset
- uspto-grants-1981_02
- Patent number
- US04251658
Reaction notes
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