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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9952생성일: 2026년 10월 24일

1,8-Diazabicyclo(5.4.0)undec-7-ene → N-[2-(2,6-Dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-ylmethyl]-acetamide

https://huagongshe.com/ko/reaction/9952

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참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물3-Aminopiperidine-2,6-dione hydrochlorideHCID 134548—
반응물3-(Acetylamino-methyl)-phthalic acid dimethyl esterHCID 21040132—
용매DimethylformamideHCID 6228—
생성물N-[2-(2,6-Dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-ylmethyl]-acetamideHCID 988052722.8%

반응 조건

온도120 °C

반응 단계

1,8-Diazabicyclo[5,4,0]undec-7-ene (0.93 g, 6 mmol) was added dropwise to a stirred suspension of 3-(acetylamino-methyl)-phthalic acid dimethyl ester (1.61 g, 6.0 mmol) and aminoglutarimide hydrochloride (1.0 g, 6.0 mmol) in DMF (15 ml). The mixture was then heated to 120° C. for 24 hours. The cooled mixture was concentrated in vacuo and the residue was stirred with water (25 ml) and dichloromethane (20 ml). The resulting slurry was filtered to give 0.45 g (22%) of the product as a gray solid. Recrystallization from methanol gave a white solid: mp 177–179° C.; 1H NMR (DMSO-d6) δ (11.02 (s, 1H), 8.36 (t, J=5.8 Hz, 1H), 7.74–7.55 (m, 3H), 5.05–4.98 (dd, J=5.3 and 12.5 Hz, 1H), 4.57 9D, j=5.9 Hz, 2H), 2.84–2.70 (m, 1H), 2.51–2.34 (m, 2H), 1.95–1.91 (m, 1H), 1.79 (s, 3H); 13C NMR (DMSO-d6) δ (172.85, 169.89, 169.81, 167.56, 167.05, 139.37, 134.83, 133.35, 131.58, 127.14, 121.94, 48.91, 37.84, 30.98, 22.54, 22.05; Anal. Calcd. For C16H15N3O5+0.96 water: C, 55.45; H, 4.92; N, 12.12. Found: C, 55.27; H, 4.82; N, 12.00.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091353B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7104d6d60d7c4909895bb7a01f22a534
출처 메모uspto-grants-2006_08