3-Chloro-6-(4-chlorophenyl)pyridazine → HCID 12726825, compound
Reaction equation
Cl[C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([Cl:14])[CH:9]=2)=[CH:6][CH:7]=1.Cl[C:16]1[N:17]=[N:18]C(C2C=CC(Cl)=CC=2)=CC=1>>[Cl:14][C:10]1[CH:9]=[C:8]([C:5]2[CH:6]=[CH:7][C:2]3[N:3]([CH:16]=[N:17][N:18]=3)[N:4]=2)[CH:13]=[CH:12][CH:11]=1Participants
3
Procedure
The procedure of Example 15 is repeated substituting an equimolecular amount of 3-chloro-6-(m-chlorophenyl)pyridazine for the 3-chloro-6-(p-chlorophenyl)pyridazine employed in that example. There is thus obtained the title compound in equally good yield; m.p. 175°-177° C.
Sources & evidence
- ORD record
- ord-0bf43f2a46594fe48eb9a57b8064ddf9
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04117130
Reaction notes
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