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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072373Generated: November 1, 2026

Acetic Acid → HCID 90902646, compound

https://huagongshe.com/reaction/1072373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantTBAF tetrahydrofuranHCID 11078149—
ReactantHCID 91366763HCID 91366763—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 90902646HCID 9090264674.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908913B2
Source datasetuspto-grants-2005_06
ORD IDord-b92d908e4ca8455096a5b21a0af670fc
Source noteuspto-grants-2005_06