Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186498Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 68226572, compound

https://huagongshe.com/reaction/1186498

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant{4-[3-(2-Methylsulfanyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-ylamino]-cyclohexyl}-carbamic acid tert-butyl esterHCID 68226965—
SolventDichloromethaneHCID 6344—
ProductHCID 68226572HCID 68226572—

Reaction Conditions

Temperature0 °C

Reaction Steps

{4-[3-(2-Methylsulfanyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester (from Example 47 supra) (150 mg, 0.323 mmol) was dissolved in dichloromethane (20 mL), then m-CPBA (134 mg, 0.659 mmol) was added slowly. The reaction mixture was stirred at 0° C. for 2 hours. The solvent was removed under reduced pressure and the solid was purified by chromatography (silica gel, 10 g, 200-300 mesh, eluting with dichloromethane:methanol, 20:1) to afford {4-[3-(2-methanesulfinyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester. (Yield 110 mg, 70.8%). LC-MS: [M+H]+ 472.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673905B2
Source datasetuspto-grants-2014_03
ORD IDord-a7955aaee7834f74aec5ffd29b152771
Source noteuspto-grants-2014_03