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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 906732생성일: 2026년 10월 24일

Chloroacetyl chloride → 2-chloro-N-[2-(2,6-dioxo-3-piperidyl)-1-oxo-isoindolin-4-yl]acetamide

https://huagongshe.com/reaction/906732

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetyl chlorideHCID 6577—
반응물LenalidomideHCID 216326—
촉매Chloroacetyl chlorideHCID 6577—
용매TetrahydrofuranHCID 8028—
생성물2-chloro-N-[2-(2,6-dioxo-3-piperidyl)-1-oxo-isoindolin-4-yl]acetamideHCID 988085992.1%

반응 단계

To a stirred suspension of 3-(4-amino-1-oxoisoindolin-2-yl)piperidine-2,6-dione (3.89 g, 15.0 mmol) in THF (50 ml) was added chloroacetyl chloride (1.86 g, 16.5 mmol). The mixture was heated to reflux for 45 minutes. To the reaction mixture was added additional chloroacetyl chloride (0.15 g, 0.13 mmol). The reaction mixture was heated at reflux for an additional 30 minutes. The solvent was evaporated in vacuo and the resulting solid was slurried in diethyl ether (20 ml) and filtered to give 4.64 g (92%) of product as an off-white solid: 1H NMR (DMSO-d6) δ 11.04 (s, 1H), 10.22 (s, 1H), 7.82 (dd, J=1.6 and 7.2 Hz, 1H), 7.59-7.50 (m, 2H), 5.16 (dd, J=5.1 and 13.2 Hz, 1H), 4.46-4.30 (m, 4H), 3.00-2.85 (m, 1H), 2.65-2.58 (m, 1H), 2.44-2.28 (m, 1H), 2.06-2.01 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08012997B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-2f31041a412e47b9932d8caa83b39814
출처 메모uspto-grants-2011_09