Hydrochloric Acid → 76606-62-7
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][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)[N:13]=[C:12]([CH3:23])[CH:11]=1)(=O)C.[ClH:24]>CO>[ClH:24].[CH3:22][O:21][C:18]1[CH:19]=[CH:20][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]([CH3:23])=[N:13]2)=[CH:16][CH:17]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-Acetyl-2[1-(4-methoxyphenyl)-3-methyl-5-pyrazolyl]amino-2-imidazoline (13.1 g.) was treated with HCl in methanol as described in Example II to give 7.9 g. of product as the HCl salt, mp 197°-198°.
Workup
- customto give 7.9 g
Sources & evidence
- ORD record
- ord-67e3cc647aa445bb82fc0051d859cc96
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04234594
Reaction notes
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