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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9985생성일: 2026년 10월 23일

Phenylacetyl chloride → N-[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]-2-phenylacetamide

https://huagongshe.com/ko/reaction/9985

반응식

참여 물질

역할이름HCID투입량
반응물Phenylacetyl chlorideHCID 7679—
반응물PomalidomideHCID 134780—
용매TetrahydrofuranHCID 8028—
생성물N-[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]-2-phenylacetamideHCID 1027174492%

반응 단계

To a stirred suspension of 4-amino-2-(2,6-dioxo(3-piperidyl))isoindoline-1,3-dione (0.55 g, 2.0 mmol) in THF (30 ml) was added 2-phenylacetyl chloride (0.62 g, 4.0 mmol). The mixture was heated to reflux for 18 hours. The solvent was evaporated in vacuo and the resulting solid was slurried in diethyl ether (20 ml) and filtered to give 0.72 g (92%) of product as an off-white solid: mp 217–218°°C.; 1H NMR (DMSO-d6) δ 11.15 (s, 1H), 9.79 (s, 1H), 8.49 (d, J=8.4 Hz, 1H), 7.82 (t, J=7.9 Hz, 1H), 7.60 (t, J=7.3 Hz, 1H), 7.41–7.27 (m, 5H), 5.13 (dd, J=5.1 and 12.7 Hz, 1H), 3.85 (s, 2H), 2.98–2.83 (m, 1H), 2.64–2.44(m, 2H), 2.08–2.04 (m, 1H); 13C NMR (DMSO-d6) δ 172.71, 170.07, 169.74, 167.60, 166.61, 136.38, 136.10, 134.70, 131.41, 129.41, 128.58, 126.97, 125.96, 118.39, 116.90, 48.89, 43.47, 30.90, 21.91; Anal. Calcd. For C21H17N3O5: C, 64.45; H, 4.38; N, 10.74. Found: C, 64.23; H, 4.34; N, 10.53.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091353B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-1e5ef2248ecb4a34aff79c6643c75f4d
출처 메모uspto-grants-2006_08