Ethyl Acetate → 5-(2-{[4-Chloro-3-(6-chloro-4-methyl-pyridin-3-yl)-benzoyl]-methyl-amino}-phenoxy)-pentanoic acid methyl ester

HRID 1848589Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1848589
[Cl:1][C:2]1[CH:18]=[CH:17][C:5]([C:6]([N:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[OH:16])[CH3:9])=[O:7])=[CH:4][C:3]=1[C:19]1[CH:20]=[N:21][C:22]([Cl:26])=[CH:23][C:24]=1[CH3:25].C[CH:28]([CH2:33][CH2:34][CH3:35])[C:29]([O:31]Br)=[O:30].[C:36]([O-])([O-])=O.[K+].[K+].C(OCC)(=O)C>CN(C=O)C>[CH3:36][O:31][C:29](=[O:30])[CH2:28][CH2:33][CH2:34][CH2:35][O:16][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[N:8]([C:6](=[O:7])[C:5]1[CH:17]=[CH:18][C:2]([Cl:1])=[C:3]([C:19]2[CH:20]=[N:21][C:22]([Cl:26])=[CH:23][C:24]=2[CH3:25])[CH:4]=1)[CH3:9]

Komponenten

6

Versuchsvorschrift

A mixture of 4-chloro-3-(6-chloro-4-methyl-pyridin-3-yl)-N-(2-hydroxy-phenyl)-N-methyl-benzamide (108 mg, 0.28 mmol), bromo methylvalerate (60 μL, 0.42 mmol) and K2CO3 (116 mg, 0.84 mmol) in DMF (1 mL) was stirred at room temperature for 14 hrs. Ethyl acetate was added and the combined organic layers were washed with water, dried over MgSO4, then purified by silica gel column chromatography eluted with ethyl acetate/hexane (1/4) up to 1/3 to yield 5-(2-{[4-chloro-3-(6-chloro-4-methyl-pyridin-3-yl)-benzoyl]-methyl-amino}-phenoxy)-pentanoic acid methyl ester 12-1 (50 mg). MS [M+H]+: 501; tR=8.52 min. (method 1)

Aufarbeitung

  1. washthe combined organic layers were washed with water
  2. dry with materialdried over MgSO4
  3. custompurified by silica gel column chromatography
  4. washeluted with ethyl acetate/hexane (1/4) up to 1/3

Quellen und Nachweise

ORD-Eintrag
ord-3f5d71019b304ff985a76080540a4fed
Quelldatensatz
uspto-grants-2015_02
Patentnummer
US08952161B2

Notizen zur Reaktion

Wird geladen…