Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 22290994 | HCID 22290994 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22290995 | HCID 22290995 | 69.3% |
Reaction Steps
To a solution of the product from Step C (0.66 g, 3.0 mmol) in dichloromethane (10 ml) at 0° C. was added triethylamine (0.55 ml, 3.9 mmol) and methanesulfonyl chloride (0.31 ml, 3.9 mmol). After stirring for 30 min, ether (50 ml) and water (50 ml) were added. The organic layer was separated and the aqueous extracted with ether (2×50 ml). The combined ether extracts were washed with brine (30 ml), dried (MgSO4), and evaporated. The residue was taken up in DMF (6 ml) and sodium azide (0.26 g, 3.9 mmol) added. This mixture was heated at 70° C. for 12 h, poured into water, and extracted with ether (3×50 ml). The combined extracts were washed with brine, dried (MgSO4), and evaporated to a residue, which was purified by chromatography (silica, hexane to 10% ethyl acetate in hexane) to give an oil (0.51 g, 69%): MS (ES) m/z 246 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06956036B1 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-bb7e33b2730a4b4cad30eac5dda35e98 |
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| Source note | uspto-grants-2005_10 |
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