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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181417Generated: October 26, 2026

Sodium Carbonate → 2-(4-Fluorophenyl)-5-aminoimidazo[4,5-b]pyridine

https://huagongshe.com/reaction/2181417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-(4-Fluorophenyl)-1-(2-methylthio-4-pyrimidinyl)-5-aminoimidazo[4,5-b]pyridineHCID 22486130—
Solvent1-Phenethylamine, (-)-HCID 75818—
SolventAcetic acid methylene chlorideHCID 21922555—
Product2-(4-Fluorophenyl)-5-aminoimidazo[4,5-b]pyridineHCID 2248613252%

Reaction Conditions

Temperature120 °C

Reaction Steps

2-(4-Fluorophenyl)-1-(2-methylthio-4-pyrimidinyl)-5-aminoimidazo[4,5-b]pyridine (110 mg, 0.31 mmol) is dissolved in CH2Cl2/HOAc 1:1 (6.2 nm), combined at 0° C. with mCPBA (84 mg 70%, 0.34 mmol) and stirred for 30 min. The reaction mixture is poured on 2N Na2CO3 and extracted with ethyl acetate three times. The combined organic phases are dried over Na3SO4, filtered and evaporated to dryness to yield the crude sulfoxide (110 mg). 50 mg are dissolved in 1-(S)-phenylethylamine (0.5 ml) and heated to 120° C. for 1 h. Purification over RP18 (CH3CN/Water 70/30 to 10/90) yielded the title compound as light brown foam (30 mg 52%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06891039B2
Source datasetuspto-grants-2005_05
ORD IDord-cad03a0fa5384ed7804d87150dcfafcf
Source noteuspto-grants-2005_05