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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253998Generated: November 2, 2026

Sodium Iodide → 2-Methyl-2-propanyl {(1S)-2-{4-[(2-methyl-1,3-thiazol-4-yl)methoxy]phenyl}-1-[(2S)-2-oxiranyl]ethyl}carbamate

https://huagongshe.com/reaction/1253998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCesium carbonateHCID 10796—
Reactant4-(Chloromethyl)-2-methyl-1,3-thiazole--hydrogen chloride (1/1)HCID 2734203—
ReactantHCID 9993752HCID 9993752—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Methyl-2-propanyl {(1S)-2-{4-[(2-methyl-1,3-thiazol-4-yl)methoxy]phenyl}-1-[(2S)-2-oxiranyl]ethyl}carbamateHCID 11618051—

Reaction Conditions

Temperature20 °C

Reaction Steps

0.6 g (3.26 mmol) 4-Chloromethyl-2-methyl-thiazole hydrochloride was added to a stirred solution of 0.76 g (2.71 mmol) tert-butyl (1S)-2-(4-hydroxyphenyl)-1-[(2S)-oxiranyl]ethylcarbamate in 15 ml N,N-dimethylformamide. 3.25 g (10 mmol) cesium carbonate and 550 mg (3.66 mmol) sodium iodide was added, and the mixture was stirred at 20° C. for 24 hours. 200 ml ethyl acetate was added, and the mixture was filtered. The filtrate was extracted with water (5×50 ml), and the organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified on silicagel column using hexane-ethyl acetate (1:1) as solvent to yield 820 mg (Y=78%) title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455497B2
Source datasetuspto-grants-2013_06
ORD IDord-7b69c33f2f084bcfb0d6bbab5b1857c7
Source noteuspto-grants-2013_06