Reacción #531863

Ecuación de reacción

4-(3-adamantan-1-yl-ureido)butyric acid

4-hydroxyphenylacetic acid

EDCI

bromoethane

K2CO3

→

852

Rendimiento 20.0%

4-(3-Adamantan-1-yl-ureido)butyric Acid 4-Ethoxycarbonylmethylphenyl Ester

Rendimiento 20.0%

Disolventes

methylene chloride

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   Lavadothe reaction mixture was washed with water (20 mL)
2. 2
   workup.DISSOLUTIONthe methylene chloride solution dissolving the product
3. 3
   Secadowas dried over Na2SO4
4. 4
   Concentraciónconcentrated
5. 5
   Otroto give
6. 6
   workup.STIRRINGstirred for 12 h at room temperature
7. 7
   ExtracciónThe ethyl ester product was extracted with ether (30 mL)
8. 8
   Lavadothe ether solution was washed with 1 N NaOH aqueous solution (20 mL) and water (30 mL)
9. 9
   Secadodried over Na2SO4
10. 10
    Concentraciónconcentrated
11. 11
    OtroThe residue was purified by column chromatography on silica gel
12. 12
    Lavadoeluting hexane and ethyl acetate (5:1)

Procedimiento

To a solution of 4-(3-adamantan-1-yl-ureido)butyric acid 822 (0.15 g, 0.54 mmol), DMAP (0.07 g, 0.54 mmol), and 4-hydroxyphenylacetic acid (0.09 g, 0.59 mmol) in methylene chloride (20 mL) was added EDCI (0.11 g, 0.59 mmol) at room temperature. After stirring for 12 h, the reaction mixture was washed with water (20 mL), and the methylene chloride solution dissolving the product was dried over Na2SO4 and concentrated to give conjugated product. This crude mixture in DMF (30 mL) was treated with bromoethane (0.15 g, 1.34 mmol) and K2CO3 (0.18 g, 1.34 mmol) at room temperature and stirred for 12 h at room temperature. The ethyl ester 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 hexane and ethyl acetate (5:1) to give 852 (47 mg, 20%) as a white solid: 1H NMR (CDCl3) 1.40 (3H, t, J=6.9 Hz), 1.66-1.68 (6H, m), 1.89-1.95 (8H, m), 2.05-2.07 (3H, m), 2.62 (2H, t, J=6.9 Hz), 3.25 (2H, q, J=6.9 Hz), 3.60 (2H, s), 4.07 (1H, s), 4.16 (2H, q, J=6.9 Hz), 4.29 (1H, s), 7.08-7.10 (2H, m), 7.28-7.30 (2H, m); LC-MS (ESI) m/z calcd for C25H34N2O5 [M+H]+ 443.25. found [M+H]+ 443.25; mp 95-97 C. Anal. (C25H34N2O5) C, H, N.

Fuente