Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 3-Methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)azetidine | HCID 22242857 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22242898 | HCID 22242898 | 55.4% |
Reaction Steps
To a solution of 3-methanesulfonyloxy-1-(p-nitrobenzyloxycarbonyl)azetidine (4.63 g, 14.0 mmol) (obtained as described in Reference Example 54(2)) in dimethylformamide (140 ml) was added sodium azide (1.37 g, 21.0 mmol), and the mixture was stirred in an oil bath (100° C.) for 4 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (2:1→1:1) as the eluant to afford 3-azido-1-(p-nitrobenzyloxycarbonyl)azetidine (2.15 g, yield 55%) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001897B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-e7bc774f853649a788db06976045a7a6 |
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| Source note | uspto-grants-2006_02 |
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