Dimethylamine → Benzophenone
Reaction equation
Cl[C:2]1[CH:3]=[CH:4][C:5](N2C(CO)=NN=C2C)=[C:6]([CH:15]=1)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:8].CS(Cl)(=O)=O.CNC.[I-].[K+]>C(N(CC)CC)C>[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:8])[C:6]1[CH:15]=[CH:2][CH:3]=[CH:4][CH:5]=1Participants
6
Procedure
In the manner given in Example 21, 5-chloro-[3-methyl-5-(hydroxymethyl)-4H-1,2,4-triazol-4-yl]benzophenone was reacted with methanesulfonyl chloride in the presence of triethylamine and the resulting solution, treated with gaseous dimethylamine in the presence of potassium iodide, to give 5-chloro-2-[3-methyl-5-(dimethylamino)methyl]-4H-1,2,4-triazol-4-yl]benzophenone of melting point 171°-172°.
Sources & evidence
- ORD record
- ord-36dd8595573c43e6bd2af3e5ff75ea46
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03993660
Reaction notes
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