Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | HCID 59396014 | HCID 59396014 | — |
| Product | HCID 86643145 | HCID 86643145 | — |
Reaction Steps
To a solution of 1,1-dimethylethyl {2-[(4S)-2,2-dimethyl-4-(2-propen-1-yl)-1,3-oxazolidin-3-yl]-2-oxoethyl}carbamate D22 (28.67 g) in DCM (300 ml) 2,6-dimethylpyridine (27.9 ml, 240 mmol) was added followed by trimethylsilyl trifluoromethanesulfonate (34.7 ml, 192 mmol) the mixture was stirred at room temperature for 30 min. The reaction was quenched with 2 ml of water and the solvent was removed under reduced pressure, the residue was charged on a Biotage 75 L column eluting with [DCM/MeOH 100:0 then 98:2 then 96:4 then 85:15]. Evaporation of the solvent gave: the title compound D23 (21 g). UPLC (Acid FINAL_QC): rt=0.36 minutes, peak observed: 199 (M+1−CHF3O3S)C10H18N2O2.CHF3O3S requires 348. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.40 (s, 3 H), 1.50 (s, 3 H), 2.17-2.43 1.40 (m, 2 H), 3.68-3.98 (m, 4 H), 3.99-4.09 (m, 1 H), 4.83-5.40 (m, 2 H), 5.58-5.97 (m, 1H), 7.63-8.36 (br.s., 2 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133908B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-a74197d466134f8fb02b23d0436c7b72 |
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| Source note | uspto-grants-2012_03 |
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