1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-[4-(3-Adamantan-1-yl-ureido)-butyryloxymethyl]-benzoic acid ethyl ester

HRID 1444646

Reaktionsgleichung

Reaktionsgleichung von HRID 1444646
[C:1]12([NH:11][C:12](=[O:20])[NH:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[CH2:21]([O:23][C:24](=[O:33])[C:25]1[CH:30]=[CH:29][C:28]([CH2:31]O)=[CH:27][CH:26]=1)[CH3:22].CCN=C=NCCCN(C)C>CN(C1C=CN=CC=1)C.C(Cl)Cl>[CH2:21]([O:23][C:24](=[O:33])[C:25]1[CH:30]=[CH:29][C:28]([CH2:31][O:18][C:17](=[O:19])[CH2:16][CH2:15][CH2:14][NH:13][C:12]([NH:11][C:1]23[CH2:8][CH:7]4[CH2:9][CH:3]([CH2:4][CH:5]([CH2:6]4)[CH2:10]2)[CH2:2]3)=[O:20])=[CH:27][CH:26]=1)[CH3:22]

Komponenten

6

Edukt 3

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 114259954-(3-Adamantan-1-yl-ureido)butyric acidHCID 12480307Ethyl 4-(hydroxymethyl)benzoate

Produkt 1

HCID 112821754-[4-(3-Adamantan-1-yl-ureido)-butyryloxymethyl]-benzoic acid ethyl esterAusbeute 76,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 142844-(Dimethylamino)pyridineKatalysatorHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 4-(3-adamantan-1-yl-ureido)butyric acid 822 (1.23 g, 0.83 mmol), DMAP (0.05 g, 0.42 mmol), and the above alcohol (0.15 g, 0.83 mmol) in methylene chloride (30 mL) was added EDCI (0.16 g, 0.83 mmol) at room temperature. After stirring for 12 h, the reaction mixture was washed with 1 N NaOH aqueous solution (15 mL) and water (30 mL), and the organic layer was dried over Na2SO4 and concentrated. Then the residue was purified by column chromatography on silica gel eluting hexane and ethyl acetate (5:1) to provide 849 (0.28 g, 75%) as a white solid: 1H NMR (CDCl3) 1.40 (3H, t, J=6.9 Hz), 1.66-1.68 (6H, m), 1.84 (2H, quint, J=6.9 Hz), 1.94-1.96 (6H, m), 2.05-2.07 (3H, m), 2.44 (2H, t, J=6.9 Hz), 3.17 (2H, q, J=6.9 Hz), 4.02 (1H, s), 4.17 (1H, s), 4.38 (2H, q, J=6.9 Hz), 5.17 (2H, s), 7.40 (2H, d, J=7.8 Hz), 8.00 (2H, d, J=7.8 Hz); LC-MS (ESI) m/z calcd for C25H34N2O5 [M+H]+ 443.25, found [M+H]+ 443.25; mp 96-99 C. Anal. (C25H34N2O5) C, H, N.

Aufarbeitung

  1. washthe reaction mixture was washed with 1 N NaOH aqueous solution (15 mL) and water (30 mL)
  2. dry with materialthe organic layer was dried over Na2SO4
  3. concentrationconcentrated
  4. customThen the residue was purified by column chromatography on silica gel
  5. washeluting hexane and ethyl acetate (5:1)

Quellen und Nachweise

ORD-Eintrag
ord-1fbf349398e7475e98d3db8730fe2772
Quelldatensatz
uspto-grants-2010_02
Patentnummer
US07662910B2

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