Acetohydrazide → HCID 12726847, compound
Reaction equation
Cl[C:2]1[N:3]=[N:4][C:5]([C:9]2[CH:10]=[C:11]([C:15]([F:18])([F:17])[F:16])[CH:12]=[CH:13][CH:14]=2)=[C:6]([CH3:8])[CH:7]=1.[C:19]([NH:22][NH2:23])(=O)[CH3:20]>C(O)CCC>[CH3:20][C:19]1[N:3]2[N:4]=[C:5]([C:9]3[CH:10]=[C:11]([C:15]([F:18])([F:17])[F:16])[CH:12]=[CH:13][CH:14]=3)[C:6]([CH3:8])=[CH:7][C:2]2=[N:23][N:22]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
As in Example 36, a mixture of 8.0 g of 3-chloro-5-methyl-6-(α,α,αtrifluoro-m-tolyl)pyridazine and 4.34 g. of acetylhydrazine in 125 ml. of n-butanol is refluxed for 48 hr. to give 6.2 g. of cream colored crystals, m.p. 185°-187° C.
Workup
- customto give 6.2 g
Sources & evidence
- ORD record
- ord-baefe6bf7e464d6cab5c70d18073a44d
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04112095
Reaction notes
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