Methylhydrazine → HCID 12582663, compound
Reaction equation
[C:1]([N:9]1[CH2:20][CH2:19][C:12]2[N:13]=[N:14][C:15](SC)=[CH:16][C:11]=2[CH2:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:21][NH:22][NH2:23]>C(O)C>[C:1]([N:9]1[CH2:20][CH2:19][C:12]2[N:13]=[N:14][C:15]([N:22]([CH3:21])[NH2:23])=[CH:16][C:11]=2[CH2:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.9 g of 6-benzoyl-5,6,7,8-tetrahydro-3-methylmercaptopyrido[4,3-c]pyridazine and 1.5 g of methylhydrazine are heated in 20 cc of 95% ethanol in an autoclave at a bath temperature of 150° for 18 hours, and the mixture is subsequently worked up as described in Example 47. The bisqentisinate of the title compound has a M.P. 166°-168° (decomp.).
Sources & evidence
- ORD record
- ord-24f7d6588d734efd823418d450f787a4
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03954754
Reaction notes
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