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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382648Generated: October 31, 2026

HCID 70150416, compound → HCID 131722927, compound

https://huagongshe.com/reaction/382648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70150416HCID 70150416—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
ProductHCID 131722927HCID 13172292769.7%

Reaction Steps

To a solution of 183.0 mg of 4-nitrobenzyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(7-hydroxymethylimidazo[5,1-b]thiazol-2-yl)-1-methyl-1-carbapen-2-em-3-carboxylate in 15 ml of dichloromethane 15 ml was added 596.7 mg of manganese dioxide, and the mixture was stirred at room temperature for 38 hours. The catalyst was removed by filtration on Celite, and the filtrate was removed under reduced pressure. The residue thus obtained was purified by column chromatography on silica gel (ethyl acetate:methanol=9:1) to give 127 mg of 127 mg of 4-nitrobenzyl (1S,5R,6S)-2-(7-formylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310056B1
Source datasetuspto-grants-2001_10
ORD IDord-30e7d747df8b4870a9d07c1e36adbf11
Source noteuspto-grants-2001_10