Pyridine → cis-2,2,2-trifluoro-1-[8-(4-methoxy-phenoxy)-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl]-ethanone

HRID 2360770Notes

Reaction equation

HRID 2360770 reaction equation
[F:1][C:2]([F:21])([F:20])[C:3]([N:5]1[C@@H:14]2[C@@H:9]([C:10]3[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][C:11]=3[CH2:12][CH2:13]2)[CH2:8][CH2:7][CH2:6]1)=[O:4].[CH3:22][O:23][C:24]1[CH:29]=[CH:28][C:27](B(O)O)=[CH:26][CH:25]=1.N1C=CC=CC=1>ClCCl.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[F:21][C:2]([F:1])([F:20])[C:3]([N:5]1[C@@H:14]2[C@@H:9]([C:10]3[CH:18]=[CH:17][C:16]([O:19][C:27]4[CH:28]=[CH:29][C:24]([O:23][CH3:22])=[CH:25][CH:26]=4)=[CH:15][C:11]=3[CH2:12][CH2:13]2)[CH2:8][CH2:7][CH2:6]1)=[O:4]

Participants

6

Reactant 3

HCID 1049PyridineHCID 201262(4-Methoxyphenyl)boronic acidHCID 86654074cis-2,2,2-trifluoro-1-(8-hydroxy-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl)-ethanone

Product 1

HCID 86654073cis-2,2,2-trifluoro-1-[8-(4-methoxy-phenoxy)-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl]-ethanone

Reagents, catalysts & solvents 2

HCID 8895Cupric acetateCatalystHCID 6344DichloromethaneSolvent2×

Procedure

A mixture of cis-2,2,2-trifluoro-1-(8-hydroxy-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl)-ethanone (0.98 g), 4-methoxyphenylboronic acid (1.00 g), pyridine (1.30 mL), copper(II) acetate (0.60 g), molecular sieves 3 Å (3.60 g), and dichloromethane (15 mL) is stirred in air at room temperature overnight. The mixture is diluted with dichloromethane and filtered over Celite. The filtrate is concentrated and the residue is chromatographed on silica gel (dichloromethane/methanol containing 1% NH3 99:1→95:5) to give the title compound as a colorless resin-like solid. Yield: 1.05 g (79% of theory); LC (method 1): tR=5.00 min; Mass spectrum (ESI+): m/z=406 [M+H]+.

Workup

  1. filtrationfiltered over Celite
  2. concentrationThe filtrate is concentrated
  3. customthe residue is chromatographed on silica gel (dichloromethane/methanol containing 1% NH3 99:1→95:5)

Sources & evidence

ORD record
ord-270f22fce93b461197abca7e0a994bec
Source dataset
uspto-grants-2014_04
Patent number
US08686149B2

Reaction notes

Loading…