HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Nitrobenzyloxycarbonylaminosulfonyl)aminoethanol → (1s,5r,6s)-6-((1r)-1-Hydroxyethyl)-1-methyl-2-[7-[1-(2-sulfamoylaminoethyl)pyridinium-3-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Nitrobenzyloxycarbonylaminosulfonyl)aminoethanol | HCID 22390400 | — |
| Reactant | (4-nitrobenzyl) (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 | HCID 68934911 | — |
| Product | (1s,5r,6s)-6-((1r)-1-Hydroxyethyl)-1-methyl-2-[7-[1-(2-sulfamoylaminoethyl)pyridinium-3-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate | HCID 10144305 | 17.7% |
Reaction Steps
The title compound (101 mg) was prepared in the same manner as in steps a) and b) of Example 4, except that 572 mg of 2-(4-nitrobenzyloxycarbonylaminosulfonyl)aminoethanol was used instead of 3-azido-1-propanol in step a) of Example 4 and 585 mg of 4-nitrobenzyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(pyridin-3-yl)carbonylimidazo[5,1-b]thiazol-2-yl]-1-carbapen-2-em-3-carboxylate was used as the starting compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06908913B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-695c5ddf3fbe443c9a8555c3b035c538 |
| Source note | uspto-grants-2005_06 |