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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575883Generated: October 29, 2026

Ammonia → Avibactam Impurity 19

https://huagongshe.com/reaction/575883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 66870454HCID 66870454—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
ProductAvibactam Impurity 19HCID 6687046387.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

230 mg (0.84 mmol) of (2R,5S)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acid was dissolved in dehydrated dichloromethane (4.2 mL), and 110 mg of triethylamine was added, followed by cooling to 0° C. 137 mg of isobutyl chloroformate was added to the mixture, followed by stirring at the same temperature for 20 minutes. 0.6 mL of aqueous ammonia was added to the reaction mixture, followed by stirring at room temperature for 1 hour. Subsequently, water (10 mL) was added and the organic layer was aliquoted, followed by sequential washing with water and saturated brine and drying over anhydrous magnesium sulfate. The residue resulting from concentration of the solvent under reduced pressure was applied to silica gel column chromatography (hexane/ethyl acetate=1/3), and subsequently crystallized with chloroform/hexane=1:3 to afford 202 mg of the title compound as a colorless crystalline powder (yield 87%). Enantiomeric excess: 99.9% ee or more (CHIRALPAK AD-H, 4.6×150 mm, hexane/ethanol=4/1, UV 210 nm, flow rate 1 mL/min., retention time 10.3 min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035062B2
Source datasetuspto-grants-2015_05
ORD IDord-101be8caca0741b2a1b77586dafaea0c
Source noteuspto-grants-2015_05