Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | TBAF tetrahydrofuran | HCID 11078149 | — |
| Reactant | HCID 91366763 | HCID 91366763 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 90902646 | HCID 90902646 | 74.5% |
Reaction Steps
Acetic acid (0.219 ml) and 1.27 ml of a 1 M tetra-n-butylammonium fluoride/THF solution were added to a solution of 369 mg of 4-nitrobenzyl (1S,5R,6S)-2-[7[(2S,4R)-4-t-butyldimethylsilyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-2-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate in 10 ml of THF, and the mixture was stirred at room temperature for 7 hr. Brine was added to the reaction solution. The mixture was adjusted to pH 8.2 by the addition of a saturated sodium hydrogencarbonate solution and was then extracted twice with ethyl acetate. The organic layers were combined, and the combined organic layers were washed with brine and were dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (dichloromethane:methanol=10:1) to give 239 mg of 4-nitrobenzyl (1S,5R,6S)-2-[7-[(2S,4R)-4-hydroxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-2-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06908913B2 |
|---|
| Source dataset | uspto-grants-2005_06 |
|---|
| ORD ID | ord-b92d908e4ca8455096a5b21a0af670fc |
|---|
| Source note | uspto-grants-2005_06 |
|---|