Reaction #1763166

ord-051901597d044e4caf9cd3efaa4e7679

Reaction equation

NCC1(CC(=O)O)CCCCC1
gabapentin
O=C([O-])O.[Na+]
sodium bicarbonate
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
compound ( 10 )
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
[(1-Isobutanoyloxyethoxy)carbonyloxy]Succinimide
CC(OC(=O)NCC1(CC(=O)O)CCCCC1)OC(=O)C(C)C
title compound ( 12 )
Yield 96.0%
CC(OC(=O)NCC1(CC(=O)O)CCCCC1)OC(=O)C(C)C
{[(1-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-1-Cyclohexane Acetic Acid
Yield 96.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Washwashed with 0.1 M aqueous potassium bisulfate (3×100 mL)
  2. 2
    OtherThe organic phase was separated
  3. 3
    Dryingdried over anhydrous magnesium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated in vacuo

Procedure

To a solution of gabapentin (1.7 g, 10 mmol) and sodium bicarbonate (20 mmol) in water (40 mL) was added a solution of compound (10) (2.73 g, 10 mmol) in acetonitrile (20 mL) over 1 min. The reaction was stirred at ambient temperature for 16 h. The reaction mixture was diluted with diethyl ether (100 mL) and washed with 0.1 M aqueous potassium bisulfate (3×100 mL). The organic phase was separated, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to afford the title compound (12) as a white solid (2.7 g, 96%). The product was recrystallized by dissolution in 1:10 ethyl acetate:heptane (10 mL) at 60° C., followed by slow cooling to 4° C. The white crystalline product was isolated by filtration. Melting point: 63-64° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08003809B2uspto-grants-2011_08