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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989884Generated: October 30, 2026

Dichloromethane → HCID 23388199, compound

https://huagongshe.com/reaction/989884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 23388233HCID 23388233—
SolventBenzeneHCID 241—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 23388199HCID 2338819927.5%

Reaction Steps

4-Nitrobenzyl(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-(7-methylthioimidazo-[5,1-b]thiazol-2-yl)-1-carbapen-2-em-3-carboxylate (109 mg) was dissolved in 10 ml of benzene at room temperature. N-Chlorosuccinimide (30 mg) and 5 mg of 2,2′-azobis(isobutyronitrile) were added to the solution. The mixture was stirred for 10 min. Dichloromethane (10 ml) and 10 ml of semisaturated brine were added thereto, followed by separation. The organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (dichloromethane:methanol=20:1) to give 32 mg of 4-nitrobenzyl(1S,5R,6S)-2-(5-chloro-7-methylthioimidazo[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 numberUS06458780B1
Source datasetuspto-grants-2002_10
ORD IDord-52bbafec2db64cf6b0c7e327e9117732
Source noteuspto-grants-2002_10