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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867641Generated: October 29, 2026

Pyridine → (+/-)-3-[(Azidophenylacetyl)amino]-3-methoxy-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium salt

https://huagongshe.com/reaction/867641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Azido-2-phenylacetyl chlorideHCID 85429—
Reactant3-Amino-3-methoxy-2-oxo-1-azetidinesulfonic acid tetrabutylammonium saltHCID 131714265—
SolventAcetonitrileHCID 6342—
Product(+/-)-3-[(Azidophenylacetyl)amino]-3-methoxy-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium saltHCID 131714272—

Reaction Conditions

Temperature-20 °C

Reaction Steps

3-Amino-3-methoxy-2-oxo-1-azetidinesulfonic acid tetrabutylammonium salt (202 mgs; see Example 74A) is dissolved in 20 ml of dry acetonitrile. To the well stirred solution at -20° C. under dry nitrogen are added dry pyridine (167 μl) and α-azidophenylacetyl chloride (96 μl). After 20 minutes, 0.5M pH 5.5 monobasic potassium phosphate buffer (12 ml) is added and the acetonitrile removed in vacuo. The aqueous residue is extracted three times with methylene chloride. The extract is dried over anhydrous sodium sulfate and evaporated in vacuo to give 281 mg of crude product as a gum. This is purified by chromatography through a column of silica gel (30 g) using methylene chloride and mixtures of methylene chloride-methanol up to 6% methanol, and yielding 231 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775670
Source datasetuspto-grants-1988_10
ORD IDord-5b21835d461b49f58c7c6bdcbbbead60
Source noteuspto-grants-1988_10