Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | HCID 68664090 | HCID 68664090 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68663473 | HCID 68663473 | 3.8% |
Reaction Steps
A solution of acetic acid (57 μl, 1.00 mmol) and N,N′-carbonyldiimidazole (195 mg, 1.20 mmol) in tetrahydrofuran (20 mL) was stirred at room temperature for 1 hr. To this reaction mixture were added 1-[4-(methylsulfinyl)phenyl]-1H-benzimidazole-6-carbohydrazide (314 mg, 1.00 mmol) and N,N-dimethylformamide (5 mL), and the resulting mixture was stirred overnight. To this reaction mixture was added a solution of p-toluenesulfonyl chloride (381 mg, 2.00 mmol) in pyridine (5 mL), and the resulting mixture was stirred at 80° C. for 24 hr. After cooling, the reaction mixture was diluted with chloroform, washed with 1M hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=4/1-0/1) and recrystallized from hexane/ethyl acetate to give the title compound (12 mg, yield 3.8%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492378B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-e86a4db125e349b7873414e090354639 |
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| Source note | uspto-grants-2013_07 |
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