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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81210생성일: 2026년 10월 25일

Sulfuric Acid → HCID 178455733, 화합물

https://huagongshe.com/reaction/81210

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참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물DimethylacetamideHCID 31374—
반응물Binap, (A+-)-HCID 634876—
반응물HCID 178455731HCID 178455731—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
촉매ZincHCID 23994—
촉매palladium(II) acetateHCID 167845—
생성물HCID 178455733HCID 178455733—

반응 조건

온도80 °C

반응 단계

In an oven-dried, nitrogen cooled flask were placed palladium(II) acetate (286 mg, 1.27 mmol) and (R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (793 mg, 1.27 mmol). N,N-dimethylacetamide (76 mL) was added and degassed for three minutes with nitrogen (sparge). Sulfuric acid (0.068 mL, 1.27 mmol) was added and degassed for three minutes with nitrogen (sparge). The flask was sealed and heated to 80° C. for 30 minutes. The mixture was cooled to room temperature and added to a separate nitrogen purged flask containing racemic 6-chloro-4-(5-chloropyridin-3-yl)-3-[1-(trans-4-methylcyclohexyl)ethyl]-3H-imidazo[4,5-c]pyridine (4.96 g, 12.7 mmol), zinc cyanide (748 mg, 6.37 mmol), and zinc (83 mg, 1.27 mmol). The flask was purged with nitrogen for five minutes and sealed and heated to 80° C. for 16 hours. The reaction mixture was cooled to room temperature, filtered, diluted with ethyl acetate, and washed with water and brine. The organic layer was dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (0-100% ethyl acetate/hexanes, linear gradient) to afford racemic 4-(5-chloropyridin-3-yl)-3-[1-(trans-4-methylcyclohexyl)ethyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile. MS ESI calc'd. for C21H22ClN5 [M+H]+ 380. found 380.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846657B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-5ab78deeba3a41b8ad0e84638ffe2dd3
출처 메모uspto-grants-2014_09