Sodium Carbonate → 5-Chloro-4-nitro-1,3-dihydro-2H-benzimidazol-2-one
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]2=[N:6][Se][N:8]=[C:4]2[C:3]=1[N+:11]([O-:13])=[O:12].[OH-].[Na+].[C:16]([O-])([O-])=[O:17].[Na+].[Na+]>Cl.I.OS([O-])(=O)=O.[Na+]>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]2[NH:6][C:16](=[O:17])[NH:8][C:4]=2[C:3]=1[N+:11]([O-:13])=[O:12]Participants
7
Reactant 3
Product 1
Reagents, catalysts & solvents 3
Procedure
A solution of 5-chloro-4-nitro-2,1,3-benzoselenadiazole from Step B (650 mg, 2.47 mmol) in conc. HCl (4 mL) and 48% aqueous HI (2 mL) was stirred at ambient temperature for 2 h. The reaction was diluted with a 1:1 saturated aqueous solution of NaHSO4 and Na2CO3 (20 mL) and then adjusted to pH 10 using 10 M aqueous NaOH. The mixture was extracted with EtOAc (3×10 mL) and the organic extracts dried over Na2SO4, filtered, and concentrated in vacuo. The resulting dark red solid was dissolved in CH3CN (4 mL) and phosgene was added (20% solution in toluene, 1.5 mL, 3.2 mmol). The reaction mixture was stirred for 1 h, then diluted with toluene. Filtration of the resultant solid gave the title compound. MS: m/z=214 (M+1).
Workup
- extractionThe mixture was extracted with EtOAc (3×10 mL)
- dry with materialthe organic extracts dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- dissolutionThe resulting dark red solid was dissolved in CH3CN (4 mL)
- additionphosgene was added (20% solution in toluene, 1.5 mL, 3.2 mmol)
- additiondiluted with toluene
- filtrationFiltration of the resultant solid
Sources & evidence
- ORD record
- ord-99ca204f1dbf4eaa8713ee4688a4432b
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696192B2
Reaction notes
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