Ammonia → 3,6-Dichloropyridazin-4-amine
Reaction equation
[Cl:1][C:2]1[N:3]=[N:4][C:5]([Cl:9])=[CH:6][C:7]=1Cl.[NH3:10]>>[NH2:10][C:7]1[CH:6]=[C:5]([Cl:9])[N:4]=[N:3][C:2]=1[Cl:1]Participants
3
Procedure
A suspension of 3,4,6-trichloropyridazine (prepared by the method of B. Kasnar et al, Nucleosides and Nucleotides, 1994, 13, 459) (10.0 g) in conc. aqueous ammonia (1 L) was heated at 75° C. for 16 h. The mixture was concentrated to a small volume and extracted several times with ethyl acetate. The extracts were washed with brine, dried and evaporated. The crude product was recrystallised from ethyl acetate to give the product (5.03 g).
Workup
- customprepared by the method of B
- concentrationThe mixture was concentrated to a small volume
- extractionextracted several times with ethyl acetate
- washThe extracts were washed with brine
- customdried
- customevaporated
- customThe crude product was recrystallised from ethyl acetate
Sources & evidence
- ORD record
- ord-cb541affb9eb4221b14af8d75c7103b1
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07141564B2
Reaction notes
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