Water → 5-chloro-2-[3-(2-chloroacetamidomethyl)-5-methyl-4H-1,2,4-triazol-4-yl]-benzophenone
Reaction equation
Br.Br.[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([N:18]2[C:22]([CH3:23])=[N:21][N:20]=[C:19]2[CH2:24][NH2:25])=[C:8]([CH:17]=1)[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:10].[Cl:26][CH2:27][C:28](Cl)=[O:29].O.C(=O)(O)[O-].[Na+]>CN(C)C=O.C(Cl)Cl>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([N:18]2[C:22]([CH3:23])=[N:21][N:20]=[C:19]2[CH2:24][NH:25][C:28](=[O:29])[CH2:27][Cl:26])=[C:8]([CH:17]=1)[C:9]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)=[O:10]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 5-chloro-2-(3-aminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone dihydrobromide (0.5 g) in dimethylformamide (3 ml), chloroacetyl chloride (0.2 g) is dropwise added under ice cooling, and the resultant mixture is stirred. The reaction mixture is allowed to stand at room temperature overnight, mixed with water (3 ml), neutralized with aqueous sodium bicarbonate and shaken with methylene chloride. The methylene chloride layer is washed with water and saturated aqueous saline solution in order, dried over sodium sulfate, and evaporated under reduced pressure to remove the solvent. The residue is recrystallized from ethyl acetate/n-hexane to give 5-chloro-2-[3-(2-chloroacetamidomethyl)-5-methyl-4H-1,2,4-triazol-4-yl]-benzophenone (0.35 g) as crystals melting at 140° to 141° C.
Workup
- washThe methylene chloride layer is washed with water and saturated aqueous saline solution in order
- dry with materialdried over sodium sulfate
- customevaporated under reduced pressure
- customto remove the solvent
- customThe residue is recrystallized from ethyl acetate/n-hexane
Sources & evidence
- ORD record
- ord-ac72621a2b5f4775b7991fc8907e2e08
- Source dataset
- uspto-grants-1979_02
- Patent number
- US04141901
Reaction notes
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