Reaction #531861

ord-95024a1bef5747ffae70da080b595045

Reaction equation

CCOC(=O)CCCCCCCCCO
alcohol
CCOC(=O)CCCCCCCCCO
10-hydroxydecanoic acid ethyl ester
O=C(O)CCCNC(=O)NC12CC3CC(CC(C3)C1)C2
4-(3-adamantan-1-yl-ureido)butyric acid
CCN=C=NCCCN(C)C.CN(C)c1ccncc1
EDCI DMAP
CCOC(=O)CCCCCCCCCOC(=O)CCCNC(=O)NC12CC3CC(CC(C3)C1)C2
880
Yield 60.0%
CCOC(=O)CCCCCCCCCOC(=O)CCCNC(=O)NC12CC3CC(CC(C3)C1)C2
10-[4-(3-Adamantan-1-yl-ureido)butyryloxy]decanoic Acid Ethyl Ester
Yield 60.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

A mixture of 10-hydroxydecanoic acid (0.25 g, 1.33 mmol; 11-hydroxyundecanoic acid for compound 881 and 12-hydroxydodecanoic acid for compound 882), ethyl bromide (0.16 g, 1.46 mmol), and lithium carbonate (0.11 g, 1.46 mmol) in DMF (25 mL) was stirred at 70 C for 6 h. Then the product was extracted with ether (30 mL), and the ether solution was washed with 1 N NaOH aqueous solution (20 mL) and water (30 mL), dried over Na2SO4, and concentrated. The residue was purified by column chromatography on silica gel eluting with hexane and ethyl acetate (3:1) to give 10-hydroxydecanoic acid ethyl ester (80 mg, 28%). This alcohol was coupled with 4-(3-adamantan-1-yl-ureido)butyric acid 822 by using EDCI/DMAP coupling reagent to give 880 (0.11 g, 60%) as a solid: 1H NMR (CDCl3) 1.24-1.32 (13H, m), 1.62-1.68 (10H, m), 1.80 (2H, quint, J=6.9 Hz), 1.94-1.97 (6H, m), 2.05-2.07 (3H, m), 2.28 (2H, t, J=6.9 Hz), 2.36 (2H, t, J=6.9 Hz), 3.16 (2H, q, J=6.9 Hz), 4.05-4.14 (5H, m), 4.25 (1H, s); LC-MS (ESI) m/z calcd for C27H46N2O5 [M+H]+ 479.34. found [M+H]+ 479.29; mp 60-61 C. Anal. Calcd for C27H46N2O5: C, 67.75; H, 9.69; N, 5.85. Found: C, 68.33; H, 9.92; N, 5.97.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08476043B2uspto-grants-2013_07