돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1093960생성일: 2026년 10월 27일

Sodium Carbonate → 5-(8-(Cyclohexylamino)imidazo[1,2-a]pyrazin-5-yl)isoindolin-1-one

https://huagongshe.com/reaction/1093960

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물1,4-DioxaneHCID 31275—
반응물5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoindolin-1-oneHCID 21955795—
반응물5-bromo-N-cyclohexylimidazo[1,2-a]pyrazin-8-amineHCID 57699487—
촉매Tetrakis palladium triphenylphosphineHCID 86600928—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물5-(8-(Cyclohexylamino)imidazo[1,2-a]pyrazin-5-yl)isoindolin-1-oneHCID 2511537837%

반응 조건

온도90 °C

반응 단계

The product of Step 1 (70 mg, 0.24 mmol), Intermediate 4 (5-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-2,3-dihydro-isoindol-1-one, 77 mg, 0.3 mmol), tetrakis palladium triphenylphosphine (69 mg, 0.06 mmol), sodium carbonate solution (1.5 M, 1.28 mL, 1.92 mmol) and dioxane (3.8 mL) are combined in a flask. The mixture is degassed with nitrogen for 10 min then sealed and heated at 90° C. for 16 h. Brine is added and the mixture is washed with dichloromethane followed by ethyl acetate. The combined organic layers are dried over MgSO4 and evaporated in vacuo to afford a brown oil. The crude material is purified by column chromatography, eluting with 5% methanolic ammonia (7 N) in dichloromethane to give a brown solid. Trituration with 1:1 toluene:diethyl ether yielded the title compound as an off-white solid (30 mg, 37%). 1H-NMR (400 MHz, d6-DMSO) =1.22-1.29 (m, 1H), 1.32-1.49 (m, 4H), 1.64 (d, 1H, J=15.2 Hz), 1.77 (d, 2H, J=12.8 Hz), 1.92 (d, 2H, J=15.2 Hz), 3.97-4.01 (1H, m), 7.33 (d, 1H, J=8.4 Hz), 7.48 (s, 1H), 7.63 (s, 1H), 7.92 (s, 1H). LCMS: Rt 2.24 min (99.6%), m/z (APCI) 348 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08133895B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-f7732c306aa049988b003a031685a98d
출처 메모uspto-grants-2012_03