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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382650Generated: October 31, 2026

HCID 131722925, compound → HCID 131722930, compound

https://huagongshe.com/reaction/382650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131722925HCID 131722925—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
ProductHCID 131722930HCID 13172293047.6%

Reaction Steps

To a solution 428 mg of 4-nitrobenzyl (5R,6S)-6-((1R)-1-hydroxyethyl)-2-(7-hydroxymethylimidazo[5,1-b]thiazol-3-yl)-1-carbapen-2-em-3-carboxylate in 30 ml of dichloromethane was added 1.03 g of manganese dioxide, and the mixture was stirred at room temperature for 18 hours. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue thus obtained was washed with diethyl ether to give 202.8 mg of 4-nitrobenzyl (5R,6S)-2-(7-formylimidazo[5,1-b]thiazol-3-yl)-6-((1R)-1-hydroxyethyl)-1-carbapen-2-em-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310056B1
Source datasetuspto-grants-2001_10
ORD IDord-883c212a342b4257867475e8ee438a3e
Source noteuspto-grants-2001_10