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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 470171생성일: 2026년 10월 24일

Triphenylphosphine → (1S,4R)-4-(4,7-difluoro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopent-2-enol

https://huagongshe.com/ko/reaction/470171

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Sodium hydrideHCID 24758—
반응물rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetateHCID 10154103—
반응물HCID 178506010HCID 178506010—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(1S,4R)-4-(4,7-difluoro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopent-2-enolHCID 58329283—

반응 조건

온도60 °C

반응 단계

4,7-difluoro-1H-imidazo[4,5-c]pyridine (1-4) (2.0 g, 12.9 mmol, 1 equiv) was dissolved in dry DMF (21 mL). Sodium hydride (542 mg, 13.5 mmol, 1.05 equiv) was carefully added. The resulting mixture was stirred at ambient temperature for 45 minutes at which point triphenylphosphine (507 mg, 1.9 mmol, 0.15 equiv), Pd-tetrakis (745 mg, 0.6 mmol, 0.05 equiv) and (1R,3S)-(+)-cis-4-cyclopentene-1,3-diol 1-acetate (3-1) (2.2 g, 15.5 mmol, 1.2 equiv) in dry THF (21 mL) were added. The mixture was stirred at 60° C. for 16 hours, then cooled to ambient temperature, diluted with 100 mL EtOAc and washed with 50 mL water. The aqueous layer was washed with EtOAc three additional times, and the combined washings were dried over MgSO4, filtered and concentrated. The crude residue was purified by reverse phase chromatography (5-95% CH3CN/water with 0.1% TFA modifier) to afford (1S,4R)-4-(4,7-difluoro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopent-2-enol (3-2) as a white solid. LRMS m/z (M+H) 238.0 found, 238.1 required.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629275B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-99a7170ad43d48d4bcf9588f4f702bd6
출처 메모uspto-grants-2014_01