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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9957생성일: 2026년 10월 24일

Water → [2-(2,6-Dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-ylmethyl]-carbamic acid benzyl ester

https://huagongshe.com/ko/reaction/9957

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물3-Aminopiperidine-2,6-dione hydrochlorideHCID 134548—
반응물Methyl-3-[(benzyloxycarbonylamino)methyl]-2-(methoxycarbonyl)benzoateHCID 21988567—
용매DimethylformamideHCID 6228—
생성물[2-(2,6-Dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-ylmethyl]-carbamic acid benzyl esterHCID 1020235324%

반응 조건

온도120 °C

반응 단계

1,8-diazabicyclo[5,4,0]undec-7-ene (0.88 g, 6 mmol) was added to a stirred suspension of methyl-3-[(benzyloxycarbonylamino)methyl]-2-(methoxycarbonyl)benzoate (2.07 g, 6 mmol) and aminoglutarimide hydrochloride (0.95 g, 6 mmol) in DMF (15 ml). The mixture was heated to 120° C. for 24 hours. The mixture was cooled to room temperature and poured into water (150 ml). The mixture was extracted with ethyl acetate (3×30 ml) and the combined ethyl acetate extracts were washed with water (2×30 ml), brine (30 ml) and dried. Solvent was removed in vacuo and the residue was purified by chromatography (dichloromethane/ethyl acetate 8 to 2) to give 0.58 g (24%) of the product as a white solid: mp 166–168° C.; 1H NMR (DMSO-d6) δ 11.15 (s, 1H), 7.99–7.71 (m, 4H), 7.37 (m, 5H), 5.19–5.12 (dd, J=5.1 and 17.4 Hz, 1H), 5.07 (s, 2H), 4.70 (d, J=5.7 Hz, 2H), 2.97–2.83 (m, 1H), 2.64–2.51 (m, 2H), 2.08–2.04 (m, 1H); 13C NMR (DMSO-d6) δ 172.55, 169.89, 167.51, 167.01, 156.55, 139.46, 137.02, 134.87, 132.89, 131.57, 128.44, 127.92, 127.83, 127.06, 121.99, 65.69, 48.89, 30.97, 22.02; Anal. Calcd. For C22H19N3O6: C, 62.70; H, 4.54; N, 9.97. Found: C, 62.53; H, 4.57; N, 9.89.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091353B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6e7757d056d64b50a575967eea16aa46
출처 메모uspto-grants-2006_08