Pyridine → HCID 118075655, compound

HRID 1051626Notes

Reaction equation

HRID 1051626 reaction equation
[Br:1][C:2]1[C:3]([OH:16])=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]([C:12](=[O:14])[CH3:13])[C@@H:7]([CH3:15])[CH2:6][CH2:5]2.[C:17]([C:20]1[CH:25]=[CH:24][C:23](B(O)O)=[CH:22][CH:21]=1)(=[O:19])[NH2:18].N1C=CC=CC=1>C([O-])(=O)C.[Cu+2].C([O-])(=O)C.ClCCl>[C:12]([N:8]1[C:9]2[C:4](=[C:3]([O:16][C:23]3[CH:24]=[CH:25][C:20]([C:17]([NH2:18])=[O:19])=[CH:21][CH:22]=3)[C:2]([Br:1])=[CH:11][CH:10]=2)[CH2:5][CH2:6][C@@H:7]1[CH3:15])(=[O:14])[CH3:13]

Participants

6

Reactant 3

HCID 1049PyridineHCID 27378114-Aminocarbonylphenylboronic acidHCID 118075679(S)-1-(6-bromo-5-hydroxy-2-methyl-3,4-dihydroquinolin-1(2H)-yl)ethanone

Product 1

HCID 118075655HCID 118075655, compoundYield 35%

Reagents, catalysts & solvents 2

HCID 8895Cupric acetateCatalystHCID 6344DichloromethaneSolvent

Procedure

A 100-mL, round-bottom flask equipped with a balloon filled with air was charged with (S)-1-(6-bromo-5-hydroxy-2-methyl-3,4-dihydroquinolin-1(2H)-yl)ethanone (0.300 g, 1.06 mmol), 4-carbamoylphenylboronic acid (0.437 g, 2.65 mmol), pyridine (1 mL), dichloromethane (40 mL), copper (II) acetate (0.580 g, 3.20 mmol) and 4 Å molecular sieves (4.0 g). The resulting mixture stirred for 3 days at room temperature. The reaction mixture was filtered, and the filtrate was concentrated under vacuum. The residue was purified by preparative thin layer chromatography (eluting with 3:1, ethyl acetate/petroleum ether) to afford (S)-4-(1-acetyl-6-bromo-2-methyl-1,2,3,4-tetrahydroquinolin-5-yloxy)benzamide (0.148 g, 35%) as yellow oil. MS (ESI, pos. ion) m/z 403, 405 [M+H]+.

Workup

  1. customA 100-mL, round-bottom flask equipped with a balloon
  2. additionfilled with air
  3. filtrationThe reaction mixture was filtered
  4. concentrationthe filtrate was concentrated under vacuum
  5. customThe residue was purified by preparative thin layer chromatography (eluting with 3:1, ethyl acetate/petroleum ether)

Sources & evidence

ORD record
ord-9488c1d401f240bbb997b9bbf420f028
Source dataset
uspto-grants-2016_07
Patent number
US09388161B2

Reaction notes

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