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HRID 10061생성일: 2026년 10월 23일

Dimethylformamide → Tert-butyl 2-(4-cyano-1-oxoisoindolin-2-yl)-4-carbamoylbutanoate

https://huagongshe.com/ko/reaction/10061

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ethyl AcetateHCID 8857—
반응물Sodium BicarbonateHCID 516892—
반응물Tert-butyl 2-(4-bromo-1-oxoisoindolin-2-yl)-4-carbamoylbutanoateHCID 21988515—
촉매ZincHCID 23994—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물Tert-butyl 2-(4-cyano-1-oxoisoindolin-2-yl)-4-carbamoylbutanoateHCID 2198860474%

반응 조건

온도120 °C

반응 단계

A mixture of tert-butyl 2-(4-bromo-1-oxoisoindolin-2-yl)-4-carbamoylbutanoate (1.2 g, 3.02 mmol), zinc cyamide (0.21 g, 1.81 mmol), tris(dibenzylideneacetone)dipalladium (0.06 g, 0.06 mmol), 1,1′-bis(diphenylphosphino)ferrocene (0.067 g, 0.12 mmol) in deoxygenated DMF (15 mL) was heated to 120° C. under N2 for 6 hours. The mixture was cooled to room temperature and poured into EtOAc (100 mL) and sat. NaHCO3 (40 mL). The EtOAc solution was washed with water (2×40 mL), brine (40 mL), and dried (MgSO4). Solvent was removed and the residue was purified by chromatography (CH2Cl2:CH3OH 97.5:2.5) to afford tert-butyl 2-(4-cyano-1-oxoisoindolin-2-yl)-4-carbamoylbutanoate (0.77 g, 74%): 1H NMR (CDCl3) δ 8.07–8.03 (dd, J=0.7 and 7.4 Hz, 1H), 7.86–7.83 (dd, J=1.0 and 7.9 Hz, 1H), 7.61 (t, J=7.6 Hz, 1H), 5.91 (s, 1H), 5.68 (s, 1H), 5.03–4.98 (m, 1H), 4.85 (d, J=17.9 Hz, 1H), 4.62 (d, J=17.9 Hz, 1H), 2.48–2.41(m, 4H), 1.46 (s, 9H); 13C NMR (CDCl3) δ 173.56, 169.21, 167.70, 145.23, 134.94, 133.11, 128.93, 128.21, 115.65, 107.86, 82.98, 63.68, 54.47, 46.55, 32.34, 27.95, 25.46.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091353B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-cb213946227849cba6cbc5d842b1724b
출처 메모uspto-grants-2006_08