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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113300Generated: November 2, 2026

HCID 57643889, compound → HCID 57643907, compound

https://huagongshe.com/reaction/2113300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57643889HCID 57643889—
SolventTolueneHCID 1140—
ProductHCID 57643907HCID 5764390779.1%

Reaction Steps

Toluene (20 ml) was added to 0.76 g of (3S,4R)-1-[allyloxycarbonyl(triphenylphosphoranylidene)methyl]-3-[(1R)-1-hydroxyethyl]-4-[(1R)-1-methyl-2-[7-(pyridin-3-yl)carbonylimidazo[5,1-b]thiazol-2-yl]-2-oxoethyl]azetidin-2-one, and the mixture was heated under reflux for 2 hr. The reaction solution was concentrated by removing the solvent, and the concentrate was purified by column chromatography on silica gel (eluted with 5 to 10% methanol/ethyl acetate). The eluate containing the contemplated product was concentrated, and the resultant solid was washed with a hexane:ethyl acetate=1:1 solution to give 0.38 g of allyl (1S,5R,6S)-6-[(1R)-1-hydroxyethyl]-2-[7-(pyridin-3-yl)carbonylimidazo[5,1-b]thiazol-2-yl]-1-methylcarbapen-2-em-3-carboxylate. This product was analyzed by NMR. The results were in agreement with the results of analysis in Example 26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524951B2
Source datasetuspto-grants-2009_04
ORD IDord-243073d8eec6428d973669255e2b60d4
Source noteuspto-grants-2009_04