Reacción #1056473

ord-580f0678d8d049afb6a0bd8bd44a62e0

Ecuación de reacción

CC(c1cccc(OCCCN)c1)N(C)C
19c
CC(c1cccc(OCCCN)c1)N(C)C
3-[3-(1-Dimethylamino-ethyl)-phenoxy]-propylamine
O=C(O)CCCC[C@@H]1CCSS1
lipoic acid
CC(c1cccc(OCCCNC(=O)CCCCC2CCSS2)c1)N(C)C
19
CC(c1cccc(OCCCNC(=O)CCCCC2CCSS2)c1)N(C)C
5-[1,2]dithiolan-3-yl-pentanoic acid {3-[3-(1-dimethylamino-ethyl)-phenoxy]-propyl}-amide

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otropurified by gravity column
  2. 2
    LavadoElution with petroleum ether/toluene/CH2Cl2/MeOH/aqueous 30% ammonia solution (6:1:1.5:1.5:0.01)

Procedimiento

5-[1,2]dithiolan-3-yl-pentanoic acid {3-[3-(1-dimethylamino-ethyl)-phenoxy]-propyl}-amide (19) was synthesized from 19c (150 mg, 0.67 mmol) and lipoic acid (210 mg, 1.02 mmol) following the procedure described for 17, and purified by gravity column. Elution with petroleum ether/toluene/CH2Cl2/MeOH/aqueous 30% ammonia solution (6:1:1.5:1.5:0.01) afforded 19 as a waxy solid; 30% yield, 1H NMR (200 MHz, CDCl3) δ 7.27 (t, J=8.2 Hz, 1H); 6.78-6.98 (m, 3H), 5.99 (br t, 1H); 4.09 (t, J=6.0 Hz, 2H); 3.21-3.62 (m, 5H), 3.05-3.19 (m, 3H), 2.40-2.53 (m, 1H), 2.32 (s, 6H), 2.22 (t, J=7.2 Hz, 2H); 1.81-2.0 (m, 3H), 1.65-1.73 (m, 4H), 1.47 (d, J=6.6 Hz, 3H); MS (ESI+) m/z 411 (M+H)+. Anal. Calculated for C21H34N2O2S2: C, 61.42; H, 8.35; N, 6.82. Found: C, 61.62; H, 8.36, N, 6.80.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07307083B2uspto-grants-2007_12