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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1623305생성일: 2026년 10월 27일

Dimethyl Sulfoxide → HCID 178510200, 화합물

https://huagongshe.com/reaction/1623305

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물5'-Chloro-2'-fluoro-6-(3-fluorobenzylamino)-2,4'-bipyridine-4-carbonitrileHCID 66936967—
반응물HCID 178511674HCID 178511674—
용매Ethyl AcetateHCID 8857—
생성물HCID 178510200HCID 17851020080.1%

반응 조건

온도105 °C

반응 단계

To a scintillation vial containing 5′-chloro-2′-fluoro-6-(3-fluorobenzylamino)-2,4′-bipyridine-4-carbonitrile (72 mg, 0.202 mmol) was added DMSO (3 ml) and trans-cyclohexane-1,4-diamine (230 mg, 2.018 mmol). The homogenous yellow reaction mixture was capped and heated to 105° C. in a oil bath for 3 hr. The reaction mixture was diluted with EtOAc and washed with sat NaHCO3, sat NaCl. The organic layer was dried Na2SO4, filtered and concentrated. The crude solid was purified by Prep HPLC and the collected fractions were combined and diluted with EtOAc and neutralized with sat NaHCO3 and then sat NaCl. The organic layer was dried over Na2SO4, filtered and concentrated to afford 2′-(trans-4-aminocyclohexylamino)-5′-chloro-6-(3-fluorobenzylamino)-2,4′-bipyridine-4-carbonitrile (73 mg, 80%). LCMS (m/z): 451.2 (MH+), retention time=0.70 min. 1H NMR (400 MHz, METHANOL-d4) d ppm 1.34-1.48 (m, 2H) 1.50-1.64 (m, 2H) 2.06-2.22 (m, 4H) 3.08-3.20 (m, 1H) 3.63-3.74 (m, 1H) 4.61 (s, 2H) 6.81 (s, 1H) 6.87 (s, 1H) 6.91-6.99 (m, 1H) 7.02 (s, 1H) 7.04-7.10 (m, 1H) 7.12-7.18 (m, 1H) 7.25-7.36 (m, 1H) 8.00 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08778951B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-394708aae3084d7e9844b24a7c6f9ac2
출처 메모uspto-grants-2014_07