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HRID 396380作成日:2026年10月24日

m-Chloroperbenzoic acid → 2-(4-Fluorophenyl)-1-(2-(1-(s)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine

https://huagongshe.com/ja/reaction/396380

反応式

関与物質

役割名称HCID仕込み量
反応物m-Chloroperbenzoic acidHCID 70297—
反応物1-Phenethylamine, (-)-HCID 75818—
反応物2-(4-Fluorophenyl)-1-(2-methylthio-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridineHCID 22486159—
溶媒Acetic acid methylene chlorideHCID 21922555—
生成物2-(4-Fluorophenyl)-1-(2-(1-(s)-phenylethyl)amino-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridineHCID 2135451935%

反応条件

温度120 °C

反応手順

2-(4-Fluorophenyl)-1-(2-methylthio-4-pyrimidinyl)-5-(4-tert.butoxycarbonyl-1-piperazinyl)imidazo[4,5-b]pyridine (106 mg, 0.2 mmol) is dissolved in CH2Cl2/HOAc 1:1 (10 ml), combined with mCPBA (113 mg 70%, 0.24 mmol) and stirred for 15 min. The reaction mixture is poured on water and extracted with CH2Cl2 three times. The combined organic phases are dried over Na2SO4. filtered and evaporated to dryness to yield the crude sulfoxide (100 mg), which is dissolved in 1-(S)-phenylethylamine (0.2 ml) and heated to 120° C. for 1 h. Purification over SiO2 (acetone/hexanes 1:1) yielded the title compound as colorless foam (45 mg 35%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06608072B1
出典データセットuspto-grants-2003_08
ORD IDord-01a57e2ac74e44b59c31bb25a522d7f1
出典メモuspto-grants-2003_08