Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Propanol | HCID 1031 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 57698947 | HCID 57698947 | — |
| Product | HCID 57699132 | HCID 57699132 | — |
Reaction Steps
Sodium hydride (12 mg) was added, while cooled with ice, to a dimethylformamide (1.2 ml) solution of the 4-chloro-N-{(1R)-1-[4-ethyl-5-(methylsulfonyl)-4H-1,2,4-triazol-3-yl]ethyl}benzenesulfonamide (Compound 182) (47 mg) obtained in Example 5 and n-propanol (0.027 ml). The mixture was stirred for 30 minutes at room temperature, and then stirred for 2 hours at 100° C. After the reaction mixture was cooled to room temperature, it was added to a saturated aqueous solution (5 ml) of ammonium chloride. The mixture was extracted with ethyl acetate (20 ml×2) and washed with a saturated aqueous solution (20 ml) of sodium chloride. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel flash column chromatography using a solvent mixture of methanol and chloroform to obtain Compound 183 (35 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022225B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-3348ace328074b2d8ae8725c4283d80c |
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| Source note | uspto-grants-2011_09 |
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