HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113300Generated: November 2, 2026
HCID 57643889, compound → HCID 57643907, compound
https://huagongshe.com/reaction/2113300
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57643889 | HCID 57643889 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57643907 | HCID 57643907 | 79.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524951B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-243073d8eec6428d973669255e2b60d4 |
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| Source note | uspto-grants-2009_04 |
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