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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851631Generated: October 30, 2026

Pyridine → (2S,3S)-3-Amino-2-methyl-4-oxo-1-azetidinesulfonic acid

https://huagongshe.com/reaction/851631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosgeneHCID 6371—
ReactantTrifluoroacetic acidHCID 6422—
Reactant(3S-trans)-4-methyl-2-oxo-3-(phenylacetylamino)-1-azetidinesulfonic acid, tetrabutylammonium saltHCID 131713000—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(2S,3S)-3-Amino-2-methyl-4-oxo-1-azetidinesulfonic acidHCID 13336134%

Reaction Conditions

Temperature-15 °C

Reaction Steps

(3S-trans)-3-[(Phenylacetyl)amino]-4-methyl-2-oxo-1-azetidinesulfonic acid, tetra-n-butylammonium salt (3.79 g) is dissolved in 70 ml of methylene chloride, cooled to -15° C. and 2.3 ml of pyridine is added. The cold mixture is treated with 5.8 ml of a 12% mixture of phosgene in benzene and stirred at -10° C. for 90 minutes. Methanol (35 ml) is added and the mixture is stirred for 30 minutes followed by the addition of 1.62 ml of trifluoroacetic acid. The reaction mixture is allowed to warm to room temperature and stirred for 16 hours. The precipitated material is collected by filtration, washed with methylene chloride and dried to yield 0.43 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04386034
Source datasetuspto-grants-1983_05
ORD IDord-05a6839c0e69449b9369abec182dd6e7
Source noteuspto-grants-1983_05