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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072421Generated: October 29, 2026

Water → HCID 22386559, compound

https://huagongshe.com/reaction/1072421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylamineHCID 7912—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 11301507HCID 11301507—
SolventChloroformHCID 6212—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 22386559HCID 22386559—

Reaction Conditions

Temperature0 °C

Reaction Steps

7-(3,4-Dimethoxy-phenyl)-5-ethylsulfanyl-imidazo[1,2-c]pyrimidine (335 mg, 1.06 mmol) was dissolved in trifluoroacetic acid (TFA, 5 ml). After 5 min the TFA was evaporated. The residue was dissolved in 10 ml CH2Cl2. The solution was cooled to 0° C. and m-CPBA (70%, 524 mg, 2.12 mmol) was added. The reaction mixture was allowed to warm to room temperature and was stirred for 5 h. Diisopropylamine (598 mg, 4.63 mmol) and thiol (254 mg, 2.28 mmol) were added and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture and extraction was carried out with CHCl3. The organic layer was washed with brine, sat. NaHCO3, brine and dried over Na2SO4. The organic layer was then concentrated to give the crude product of 7-(3,4-Dimethoxy-phenyl)-5-(pyridin-4-ylsulfanyl)-imidazo[1,2-c]pyrimidine which was purified by column chromatography (160 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911443B2
Source datasetuspto-grants-2005_06
ORD IDord-82a2d923d73b444f8fab364227d66053
Source noteuspto-grants-2005_06