Oxalic Acid → 1-(4-Indolyloxy)-4-(4-(2-naphthyl)piperidin-1-yl)butane ethanedioate

HRID 481634Notes

Reaction equation

HRID 481634 reaction equation
Cl[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH:9]=[CH:10][NH:11]2.[CH:16]1[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH:19]=[CH:18][C:17]=1[CH:26]1[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]1.C(=O)([O-])[O-].[K+].[K+].[C:38]([OH:43])(=[O:42])[C:39]([OH:41])=[O:40]>C(#N)C.C(OCC)(=O)C>[C:38]([OH:43])(=[O:42])[C:39]([OH:41])=[O:40].[NH:11]1[C:12]2[C:8](=[C:7]([O:6][CH2:5][CH2:4][CH2:3][CH2:2][N:29]3[CH2:30][CH2:31][CH:26]([C:17]4[CH:18]=[CH:19][C:20]5[C:25](=[CH:24][CH:23]=[CH:22][CH:21]=5)[CH:16]=4)[CH2:27][CH2:28]3)[CH:15]=[CH:14][CH:13]=2)[CH:9]=[CH:10]1

Participants

7

Reactant 4

HCID 971Oxalic AcidHCID 11430Potassium CarbonateHCID 115721114-(4-chlorobutoxy)-1H-indoleHCID 220292644-(Naphthalen-2-yl)piperidine

Product 1

HCID 867500031-(4-Indolyloxy)-4-(4-(2-naphthyl)piperidin-1-yl)butane ethanedioate

Reagents, catalysts & solvents 2

HCID 6342AcetonitrileSolventHCID 8857Ethyl AcetateSolvent2×

Procedure

A solution of 1-chloro-4-(4-indolyloxy)butane (prepared from 4-hydroxy-1H-indole and 1-bromo-4-chlorobutane), 4-(2-naphthyl)piperidine and 3 equivalents of potassium carbonate in acetonitrile was heated at reflux for 12 h. The mixture was cooled and diluted with ethyl acetate, and the organic layer was separated and washed with brine. The crude residue was purified by silica gel chromatography (dichloromethane/5% methanol in dichloromethane gradient eluent). The resulting free base was dissolved in ethyl acetate and precipitated with one equivalent of oxalic acid in ethyl acetate, to give the title compound in 48% overall yield as a tan solid. mp . 113°-115° C. FDMS m/e=398 (M+ of free base).

Workup

  1. temperatureat reflux for 12 h
  2. temperatureThe mixture was cooled
  3. customthe organic layer was separated
  4. washwashed with brine
  5. customThe crude residue was purified by silica gel chromatography (dichloromethane/5% methanol in dichloromethane gradient eluent)
  6. dissolutionThe resulting free base was dissolved in ethyl acetate

Sources & evidence

ORD record
ord-925eb96c145e40e4bb7b1d2e4e00bd9c
Source dataset
uspto-grants-1998_08
Patent number
US05789402

Reaction notes

Loading…