돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81083생성일: 2026년 10월 24일

Dimethylacetamide → (R)-4-((1-cyclobutylethyl)amino)-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile

https://huagongshe.com/ko/reaction/81083

반응식

참여 물질

역할이름HCID투입량
반응물DimethylacetamideHCID 31374—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물(R)-6-chloro-N-(1-cyclobutylethyl)-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridin-4-amineHCID 86724459—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
촉매Palladium, di-mu-chlorobis(eta3-2-propenyl)di-HCID 61538—
생성물(R)-4-((1-cyclobutylethyl)amino)-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrileHCID 86724463—

반응 조건

온도70 °C

반응 단계

A vial containing 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (67.6 mg, 0.142 mmol) and allylpalladium(II) chloride dimer (26 mg, 0.071 mmol) in DMA (400 ul) was evacuated and refilled with Ar (3×). The resulting solution was warmed to 70° C. for 20 minutes. In a separate vial was added zinc cyanide (92 mg, 0.78 mmol), (R)-6-chloro-N-(1-cyclobutylethyl)-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridin-4-amine (290 mg, 0.71 mmol) and DMA (500 uL). The mixture was degassed with Ar for 15 minutes, and the catalyst solution was added to the mixture. The resulting mixture was stirred at 120° C. overnight. The mixture was cooled to room temperature and concentrated. The residue was dissolved in DCM purified by silica gel chromatography (0-100% ethyl acetate/hexanes, linear gradient) to give (R)-4-((1-cyclobutylethyl)amino)-3-(4-(trifluoromethyl)benzyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile. MS ESI calc'd for C21H20F3N5 [M+H]+ 400. found 400.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846657B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-138033f8ee2c457084e3eec78bd2a47b
출처 메모uspto-grants-2014_09