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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2181420생성일: 2026년 10월 25일

Acetic Acid → 2-(4-Fluorophenyl)-1-(2-cyclopentylamino-4-pyrimidinyl)-5-(benzylamino)imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/2181420

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물BenzylamineHCID 7504—
반응물5-Chloro-2-(4-fluorophenyl)-1-(2-cyclopentylamino-4-pyrimidinyl)imidazo[4,5-b]pyridineHCID 22486152—
반응물Sodium t-butoxideHCID 23676156—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매O-XyleneHCID 7237—
생성물2-(4-Fluorophenyl)-1-(2-cyclopentylamino-4-pyrimidinyl)-5-(benzylamino)imidazo[4,5-b]pyridineHCID 989129250%

반응 조건

온도160 °C

반응 단계

2-(4-Fluorophenyl)-1-(2-cyclopentylamino-4-pyrimidinyl)-5-(chloro)imidazo[4,5-b]pyridine (100 mg; 0.25 mmol), R-(+)-BINAP (10 mg; 0.016 mmol), Pd2(dba)3 (22 mg; 0.024 mmol) are suspended in xylene (16 ml), benzylamine (0.53 ml; 4.9 mmol) is added, followed by NaOtBu (47 mg; 0.49 mmol) and heated to 160° C. for 10 min. under argon. The reaction mixture is poured on water (100 ml) containing HOAc (2 ml) and extracted with TBME three times. The combined organic phases are washed with 2N Na2CO3, dried over Na2SO4 and evaporated to dryness. Purification via SiO2 chromatography (TBME/hexane 6:4 to 10:0) and recrystalisation from TBME yields the title compound as colorless crystals (50 mg. 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06891039B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-2ab1606ce7f9427aa6d580b640dc68d6
출처 메모uspto-grants-2005_05