Methyl iodide → HCID 86584524, compound

HRID 1017226Notes

Reaction equation

HRID 1017226 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([CH:28]=[CH:29][CH:30]=1)[O:6][C:7]1[N:12]=[C:11]([O:13][C:14]2[CH:15]=[C:16]([CH2:20][CH2:21][C:22]([OH:24])=[O:23])[CH:17]=[CH:18][CH:19]=2)[C:10]([F:25])=[C:9]([CH3:26])[C:8]=1[F:27])#[N:2].CI.N1(C2CCCCCCCCCC2)CCCCCCCC[CH2:35]N1>C(Cl)Cl>[C:1]([C:3]1[CH:4]=[C:5]([CH:28]=[CH:29][CH:30]=1)[O:6][C:7]1[N:12]=[C:11]([O:13][C:14]2[CH:15]=[C:16]([CH2:20][CH2:21][C:22]([O:24][CH3:35])=[O:23])[CH:17]=[CH:18][CH:19]=2)[C:10]([F:25])=[C:9]([CH3:26])[C:8]=1[F:27])#[N:2]

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 23441739HCID 23441739, compoundHCID 57346892Diazabicycloundecane

Product 1

HCID 86584524HCID 86584524, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To 3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzene-propionicacid (0.50 g, 1.2 mmol) in methylene chloride (20 mL) was added methyl iodide (0.26 g, 1.8 mmol) and diazabicycloundecane (2.8 g, 1.8 mmol). After stirring for 15 hours, the solution was concentrated in vacuo and chromatographed on silica gel with ethyl acetate/hexane (1/4) to give 3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzenepropionic acid, methyl ester; NMR (CDCl3) 7.3 (m, 5), 7.05 (d, 1), 6.85 (m, 2), 3.68 (s, 3), 2.9 (t, 2), 2.55 (t, 2), 2.4 (s, 3) ppm;

Workup

  1. concentrationthe solution was concentrated in vacuo
  2. customchromatographed on silica gel with ethyl acetate/hexane (1/4)

Sources & evidence

ORD record
ord-d06f6301441b471c9bb7aa469ab4f4aa
Source dataset
uspto-grants-2002_11
Patent number
US06479485B2

Reaction notes

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