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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072396Generated: November 2, 2026

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

https://huagongshe.com/reaction/1072396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Nitrobenzyloxycarbonylaminosulfonyl)aminoethanolHCID 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-carboxylateHCID 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-carboxylateHCID 1014430517.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908913B2
Source datasetuspto-grants-2005_06
ORD IDord-695c5ddf3fbe443c9a8555c3b035c538
Source noteuspto-grants-2005_06