Reacción #502116

ord-cafb183cfe114494a12a49cc726c2c66

Ecuación de reacción

COc1ccc2cc([C@H](C)C(=O)O)ccc2c1
(2S)-2-(6-methoxy(2-naphthyl))propanoic acid
O=[N+]([O-])C(CO)(CO)CO
2-hydroxymethyl-2-nitro-1,3-propanediol
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
CCN(C(C)C)C(C)C
NEt(i-Pr)2
COc1ccc2cc([C@H](C)C(=O)OCC(CO)(CO)[N+](=O)[O-])ccc2c1
title compound
Rendimiento 39.0%
COc1ccc2cc([C@H](C)C(=O)OCC(CO)(CO)[N+](=O)[O-])ccc2c1
3-Hydroxy-2-(hydroxymethyl)-2-nitropropyl (2S)-2-(6-methoxy(2-naphthyl))propanoate
Rendimiento 39.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was evaporated to dryness
  2. 2
    Otrothe residue was partitioned between 3N HCl (100 mL) and CH2Cl2 (200 mL×2)
  3. 3
    LavadoThe combined organic layer was back washed with water and brine
  4. 4
    Secadodried over Na2SO4
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated
  7. 7
    Otrodried under vacuum
  8. 8
    OtroThe product was separated by silica gel column chromatography
  9. 9
    Lavadoeluting with ethyl acetate/hexane (gradient from 1:2 to 1:1, Rf=0.1 in 1:2)

Procedimiento

A solution of (2S)-2-(6-methoxy(2-naphthyl))propanoic acid (naproxen, 4.27 g, 18.5 mmol), 2-hydroxymethyl-2-nitro-1,3-propanediol (2.89 g, 19.1 mmol), N,N-dimethylaminopyridine (DMAP, 0.88 g, 7.2 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (4.86 g, 25.4 mmol) and NEt(i-Pr)2 (11 mL, 63.2 mmol) in acetone (100 mL) was stirred at ambient temperature overnight. The reaction mixture was evaporated to dryness and the residue was partitioned between 3N HCl (100 mL) and CH2Cl2 (200 mL×2). The combined organic layer was back washed with water and brine, dried over Na2SO4, filtered, concentrated and dried under vacuum. The product was separated by silica gel column chromatography eluting with ethyl acetate/hexane (gradient from 1:2 to 1:1, Rf=0.1 in 1:2) to give the title compound as a white solid (2.48 g, 39% yield). Mp 124-126° C. 1H NMR (300 MHz, 10% CD3OD/CDCl3) δ 7.73-7.64 (m, 3H), 7.37-7.33 (m, 1H), 7.17-7.12 (m, 2H), 4.44 (d, J=2.6 Hz, 2H), 3.92 (s, 3H), 3.9-3.7 (m, 5H), 3.4 (br, 2H), 1.58 (d, J=7.2 Hz, 3H), 13C NMR (75 MHz, 10% CD3OD/CDCl3) δ 174.1, 157.4, 134.5, 133.5, 129.0, 128.6, 127.0, 125.7, 118.8, 105.4, 92.4, 61.2, 60.1, 55.0, 45.0, 17.7.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08088762B2uspto-grants-2012_01