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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (3S-trans)-4-methyl-2-oxo-3-(phenylacetylamino)-1-azetidinesulfonic acid, tetrabutylammonium salt | HCID 131713000 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S,3S)-3-Amino-2-methyl-4-oxo-1-azetidinesulfonic acid | HCID 133361 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04386034 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-05a6839c0e69449b9369abec182dd6e7 |
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| Source note | uspto-grants-1983_05 |
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