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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382634Generated: October 31, 2026

Iodomethyl pivalate → Pivaloyloxymethyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-5-yl)-1-methyl-1-carbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/382634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodomethyl pivalateHCID 104401—
ReactantPotassium (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-5-yl)-1-methyl-1-carbapen-2-em-3-carboxylateHCID 131722907—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductPivaloyloxymethyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-5-yl)-1-methyl-1-carbapen-2-em-3-carboxylateHCID 12070022112.1%

Reaction Steps

To a solution of 40 mg of potassium (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-5-yl)-1-methyl-1-carbapen-2-em-3-carboxylate in 0.8 ml of DMF was added at −30° C. 30 mg of pivaloyloxymethyl iodide, and the mixture was stirred for 1 hour during which the temperature was raised up to room temperature. The reaction mixture was diluted with 30 ml of dichloromethane, washed with semi-saturated aqueous saline, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue thus obtained was purified by column chromatography on silica gel (ethyl acetate:methanol=4:1) to give 54 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310056B1
Source datasetuspto-grants-2001_10
ORD IDord-0e448e43c7c3471a8f8c57b83fecc573
Source noteuspto-grants-2001_10