Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 86628908 | HCID 86628908 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 86628909 | HCID 86628909 | — |
Reaction Steps
Following the general procedure for the preparation of azides of Description 16, 23.0 g (45.3 mmol) of (methylethoxycarbonyloxy)ethyl (2R)-4-[(3-chloropropyl)sulfonyloxy]-3,3-dimethyl-2-(phenylmethoxy)butanoate (40a) dissolved in 210 mL of anhydrous dimethyl sulfoxide (DMSO) was reacted with 5.9 g (93.6 mmol) of sodium azide (NaN3). After work-up, the crude title compound (40b) was obtained and used in the next step without further purification. Rf=0.29 (EtOAc/Hxn=1:4). 1H NMR (400 MHz, CDCl3, both diastereomers): δ=1.06-1.08 (m, 6H), 1.24-1.35 (m, 6H), 1.57 (d, J=5.2 Hz, 3H), 2.03-2.10 (m, 2H), 3.10-3.16 (m, 2H), 3.44-3.48 (m, 2H), 3.84-3.85 (2s, 1H), 3.94-3.96 (2d, J=8.8, 9.2 Hz, 1H), 4.18-4.22 (2d, J=9.2, 9.6 Hz, 1H), 4.33-4.38 (2d, J=11.2, 11.2 Hz, 1H), 4.64 (t, J=11.2 Hz, 1H), 4.78-4.97 (m, 1H), 6.82-6.87 (m, 1H), 7.32-7.37 (m, 5H) ppm. MS (ESI) m/z 538.07 (M+Na)+. The analytical data was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08168617B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-d4abcc5ec93748eea523578cf319eb33 |
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| Source note | uspto-grants-2012_05 |
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