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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279816Generated: October 26, 2026

2-Azetidinone → (S)-3-Amino-N-[(methylamino)sulfonyl]-2-oxo-1-azetidinecarboxamide

https://huagongshe.com/reaction/279816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AzetidinoneHCID 136721—
ReactantBistrimethylsilylacetamidHCID 11708267—
Reactant(S)-N-[(Methylamino)sulfonyl]-2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinecarboxamideHCID 54005555—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetonitrileHCID 6342—
Product(S)-3-Amino-N-[(methylamino)sulfonyl]-2-oxo-1-azetidinecarboxamideHCID 54209056—

Reaction Steps

(S)-N-[(Methylamino)sulfonyl]-2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinecarboxamide (2.1 g; see Example 37) was suspended in 25 ml of acetonitrile and bis(trimethylsilyl)acetamide (3.3 g) was added. The solution was added to a suspension of 1 g of 10% palladium on charcoal in 25 ml of acetonitrile, through which hydrogen was passed for 30 minutes prior to the addition of the solution of the starting azetidinone. After 15 minutes the catalyst was removed by filtration and 2 ml of methanol was added to the filtrate to precipitate 1.3 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04587047
Source datasetuspto-grants-1986_05
ORD IDord-bd09386979e9458aa5f5a4ecf6bb29a4
Source noteuspto-grants-1986_05