Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 24855903 | HCID 24855903 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 24856141 | HCID 24856141 | 79.3% |
Reaction Steps
To a solution of 79 mg (0.20 mmol) of N-(4-tert-butyl-thiazol-2-yl)-2-(6-chloro-pyridine-3-sulfonyl)-2-methyl-propionamide (example 265, Table 19) and 57.5 mg (0.42 mmol) of potassium carbonate in dioxane (2 mL) were added 27 μL (0.4 mmol) of azetidine. The reaction was heated in a sealed tube to 70° C. for 3 h. The solids were removed by filtration and rinsed with dioxane (5 mL). The filtrate was concentrated under reduced pressure and the residue purified by column chromatography (silica, eluent DCM, 5-10% ethyl acetate) to afford 67 mg of 2-(6-azetidin-1-yl-pyridine-3-sulfonyl)-N-(4-tert-butyl-thiazol-2-yl)-2-methyl-propionamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935715B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-945626f82d2f43d3b37afa1c07cc84b4 |
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| Source note | uspto-grants-2011_05 |
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