Chloroacetic Acid → 2-(chloromethyl)-5-fluoro-1-methyl-1H-benzo[d]imidazole
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([NH:8][CH3:9])=[CH:6][CH:7]=1.[Cl:11][CH2:12][C:13](O)=O>>[Cl:11][CH2:12][C:13]1[N:8]([CH3:9])[C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][C:4]=2[N:10]=1Participants
3
Procedure
The title compound was prepared in accordance with the general method of Example 191(C), from 4-fluoro-N1-methylbenzene-1,2-diamine (2.5 g, 17.84 mmol) and 2-chloroacetic acid (2.50 g, 27 mmol). The crude residue was purified over silicagel chromatography (prepacked 70 g silicagel column, Cyclohexane/AcOEt: 60/40 as eluent) to afford 277 mg of 2-(chloromethyl)-5-fluoro-1-methyl-1H-benzo[d]imidazole (Yield: 8%) as a semi-solid.
Workup
- customThe crude residue was purified over silicagel chromatography (prepacked 70 g silicagel column, Cyclohexane/AcOEt: 60/40 as eluent)
Sources & evidence
- ORD record
- ord-d850dfb099c24e569f69b519015833c7
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08101637B2
Reaction notes
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