Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | 2-(1-(2,3-Dimethylphenyl)ethyl)-1H-imidazole | HCID 21662542 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57718403 | HCID 57718403 | — |
Reaction Steps
To a solution of the compound of Example 1 (100 mg, 0.5 mmol) and triethylamine (77 μl, 0.55 mmol) in anhydrous tetrahydrofuran (4 ml), was added dimethylsulphamoyl chloride (59 μl, 0.55 mmol). The reaction mixture was stirred at 60° C., under nitrogen, for 36 h and then concentrated in vacuo. The residue was partitioned between water (10 ml) and ethyl acetate (10 ml) and the two layers were separated. The aqueous layer was extracted with ethyl acetate (10 ml) and the combined organic layers were dried (MgSO4) and concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825149B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-c49d7063f1c44226bb48cc8abcefdd27 |
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| Source note | uspto-grants-2010_11 |
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