Methylhydrazine → HCID 12582663, Verbindung
Reaktionsgleichung
[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]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
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 biscentisinate of the title compound has a M.P. of 166°-168° (decomp.).
Quellen und Nachweise
- ORD-Eintrag
- ord-bdd48f5d91a246508d9a4970281c2b2e
- Quelldatensatz
- uspto-grants-1984_10
- Patentnummer
- US04478837
Notizen zur Reaktion
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