Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Methanesulfonic anhydride | HCID 81560 | — |
| Reactant | HCID 69565154 | HCID 69565154 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86759656 | HCID 86759656 | 39% |
Reaction Steps
To a solution of the product from Step A (0.14 g, 0.61 mmol) and triethylamine (0.18 g, 1.8 mmol) in anhydrous THF (50 ml) at 0° C. was added methanesulfonic anhydride (0.16 g, 0.92 mmol). The mixture was stirred for 10 min and sodium azide (0.40 g, 6.1 mmol) was added; the solvent was evaporated and anhydrous DMF (50 mL) added followed by heating at 110° C. for 3 h. The mixture was cooled, poured into a saturated solution of sodium bicarbonate (80 mL) and extracted with ethyl acetate (3×60 mL). The combined extracts were dried, filtered, and evaporated to a residue which was purified by chromatography (silica, 10% ethyl acetate in hexane) to give an oil (0.06 g, 39%): LC/MS (+APCI) m/z 256 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696476B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-30e091a819d348769a149ad774f4eee8 |
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| Source note | uspto-grants-2004_02 |
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