Dimethylformamide → 8-Chloro-3-(difluoromethoxy)-1,5-naphthyridine

HRID 40369

Reaction equation

HRID 40369 reaction equation
Cl[C:2]([F:7])([F:6])C([O-])=O.[Na+].[Cl:9][C:10]1[CH:11]=[CH:12][N:13]=[C:14]2[C:19]=1[N:18]=[CH:17][C:16]([OH:20])=[CH:15]2.C(=O)([O-])[O-].[Cs+].[Cs+].CN(C=O)C>CO.ClCCl>[Cl:9][C:10]1[CH:11]=[CH:12][N:13]=[C:14]2[C:19]=1[N:18]=[CH:17][C:16]([O:20][CH:2]([F:6])[F:7])=[CH:15]2

Participants

6

Reactant 4

HCID 6228DimethylformamideHCID 10796Cesium carbonateHCID 2734985Sodium chlorodifluoroacetateHCID 1357435768-Chloro-1,5-naphthyridin-3-ol

Product 1

HCID 576912918-Chloro-3-(difluoromethoxy)-1,5-naphthyridineYield 56%

Reagents, catalysts & solvents 1

HCID 21226129Dichloromethane methanolSolvent

Procedure

A round bottom flask under nitrogen atmosphere was charged with sodium 2-chloro-2,2-difluoroacetate (0.49 g, 3.2 mmol), 8-chloro-1,5-naphthyridin-3-ol (0.25 g, 1.4 mmol), cesium carbonate (1.4 g, 4.2 mmol), and DMF (2.8 mL, 0.5M). This was then placed in a 100° C. preheated oil bath and stirred at this temperature for 3 hours. Reaction mixture diluted with 10% Methanol/Dichloromethane and filtered over celite. Filtrate concentrated and purified by ISCO silica gel chromatography (40 g) in 1% MeOH/DCM to afford pure 8-chloro-3-(difluoromethoxy)-1,5-naphthyridine (0.18 g, 56% yield) as white solid. MS [M+H]=231.2. Calc'd for C9H5ClF2N2O=230.60.

Workup

  1. customThis was then placed in a 100° C.
  2. customReaction mixture
  3. filtrationfiltered over celite
  4. concentrationFiltrate concentrated
  5. custompurified by ISCO silica gel chromatography (40 g) in 1% MeOH/DCM

Sources & evidence

ORD record
ord-3a8bb732173e4d62bc01ee4493246dde
Source dataset
uspto-grants-2013_09
Patent number
US08524900B2

Linked notes

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