반응 #993883

반응 방정식

water

1,8-diazabicyclo[5,4,0]undec-7-ene

methyl-3-[(benzyloxycarbonylamino)methyl]-2-(methoxycarbonyl)benzoate

aminoglutarimide hydrochloride

→

product

수율 24.0%

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

수율 24.0%

용매

DMF

반응 조건

후처리

1. 1
   온도The mixture was cooled to room temperature
2. 2
   추출The mixture was extracted with ethyl acetate (3×30 ml)
3. 3
   세척the combined ethyl acetate extracts were washed with water (2×30 ml), brine (30 ml)
4. 4
   기타dried
5. 5
   기타Solvent was removed in vacuo
6. 6
   기타the residue was purified by chromatography (dichloromethane/ethyl acetate 8 to 2)

실험 절차

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 172.85, 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.

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