HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-nitrobenzyl (1R,3R,5R,6S)-6-[(R)-1-hydroxyethyl]-2-oxo-1-methylcarbapenam-3-carboxylate → HCID 91086797, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-nitrobenzyl (1R,3R,5R,6S)-6-[(R)-1-hydroxyethyl]-2-oxo-1-methylcarbapenam-3-carboxylate | HCID 13504349 | — |
| Reactant | HCID 22390333 | HCID 22390333 | — |
| Product | HCID 91086797 | HCID 91086797 | 71.6% |
Reaction Steps
4-Nitrobenzyl (1S,5R,6S)-2-[7-[1-(3-azidopropyl)piperidin-4-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate (862 mg) was prepared in the same manner as in step a) of Example 1, except that 658 mg of 4-nitrobenzyl (1R,3R,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-oxo-1-carbapenam-3-carboxylate and 1.16 g of 7-[1-(3-azidopropyl)piperidin-4-yl]carbonyl-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole were used as the starting compounds.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06908913B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-e0e58513e87940dabaed643b15921ca6 |
| Source note | uspto-grants-2005_06 |