Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | allyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylate | HCID 11046746 | — |
| Reactant | HCID 18319501 | HCID 18319501 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 131723117 | HCID 131723117 | — |
Reaction Steps
A solution of allyl (1S,5R,6S)-6-[1(R)-allyloxycarbonyloxy-ethyl]-2-hydroxymethyl-1-methyl-carbapen-2-em-3-carboxylate (365 mg, 1.0 mmol), triphenylphosphine (315 mg, 1.2 mmol), and 4-phenyl-6-(2-triethylsilanyloxy-ethyl)-2H-1-thia-2,3-diaza-naphthalene 1,1-dioxide (458mg, 1.1 mmol) in anhydrous tetrahydrofuran (7 mL) is cooled in an ice-bath and stirred under a nitrogen atmosphere while diisopropyl azodicarboxylate (0.24 mL, 1.2 mmol) is added dropwise over a few minutes. The resulting solution is stirred in the cold for 30 minutes, then diluted with chloroform, washed with 5% aqueous sodium bicarbonate and brine, dried over sodium sulfate, filtered and evaporated under vacuum. The residue is purified by silica gel flash chromatography, eluting with hexane-ethyl acetate, to afford allyl (1S,5R,6S)-6-[(1(R)-allyloxycarbonyloxy-ethyl]-2-[1,1-dioxo-4-phenyl-6-(2-triethylsilanyloxy-ethyl)-2H-1-thia-2,3-diaza-naphthalen-2-ylmethyl]-1-methyl-carbapen-2-em-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06346525B1 |
|---|
| Source dataset | uspto-grants-2002_02 |
|---|
| ORD ID | ord-a8838effeba74502b60c99e37ec31342 |
|---|
| Source note | uspto-grants-2002_02 |
|---|