Hydrochloric Acid → HCID 70592367, compound
Reaction equation
C([N:4]1[CH2:8][CH2:7][N:6]=[C:5]1[NH:9][C:10]1[N:14]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([Cl:21])[CH:16]=2)[N:13]=[C:12]([CH3:22])[CH:11]=1)(=O)C.Cl>CO>[ClH:21].[Cl:21][C:17]1[CH:16]=[C:15]([N:14]2[C:10]([NH:9][C:5]3[NH:6][CH2:7][CH2:8][N:4]=3)=[CH:11][C:12]([CH3:22])=[N:13]2)[CH:20]=[CH:19][CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-Acetyl-2-[1-(3-chlorophenyl)-3-methyl-5-pyrazolyl] amino-2-imidazoline (19.7 g.) was treated with HCl in methanol as described in Example II to give 6.5 g. product as the HCl salt, mp 208°-209°.
Workup
- customto give 6.5 g
Sources & evidence
- ORD record
- ord-a23c9b8480934240b78fa09cc7c298d5
- Source dataset
- uspto-grants-1980_10
- Patent number
- US04226773
Reaction notes
Loading…