2-(4-Iodophenoxy)-5-ethylpyrimidine → (E)-2-(2,6-dichlorobenzamido)-5-[4-(5-ethylpyrimidin-2-yloxy)phenyl]pent-4-enoic acid methyl ester

HRID 230340

Reaktionsgleichung

Reaktionsgleichung von HRID 230340
[CH3:1][O:2][C:3](=[O:19])[CH:4]([NH:8][C:9](=[O:18])[C:10]1[C:15]([Cl:16])=[CH:14][CH:13]=[CH:12][C:11]=1[Cl:17])[CH2:5][CH:6]=[CH2:7].I[C:21]1[CH:35]=[CH:34][C:24]([O:25][C:26]2[N:31]=[CH:30][C:29]([CH2:32][CH3:33])=[CH:28][N:27]=2)=[CH:23][CH:22]=1>>[CH3:1][O:2][C:3](=[O:19])[CH:4]([NH:8][C:9](=[O:18])[C:10]1[C:11]([Cl:17])=[CH:12][CH:13]=[CH:14][C:15]=1[Cl:16])[CH2:5]/[CH:6]=[CH:7]/[C:21]1[CH:22]=[CH:23][C:24]([O:25][C:26]2[N:27]=[CH:28][C:29]([CH2:32][CH3:33])=[CH:30][N:31]=2)=[CH:34][CH:35]=1

Komponenten

3

Edukt 2

HCID 577625172-(4-Iodophenoxy)-5-ethylpyrimidineHCID 577625182-(2,6-Dichlorobenzamido)pent-4-enoic acid methyl ester

Produkt 1

HCID 57762629(E)-2-(2,6-dichlorobenzamido)-5-[4-(5-ethylpyrimidin-2-yloxy)phenyl]pent-4-enoic acid methyl esterAusbeute 75,1 %

Versuchsvorschrift

In the same manner as in Example 1, 2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl ester (50.0 mg) was reacted with 2-(4-iodophenoxy)-5-ethylpyrimidine (54.1 mg) to obtain (E)-2-(2,6-dichlorobenzamido)-5-[4-(5-ethylpyrimidin-2-yloxy)phenyl]pent-4-enoic acid methyl ester (62.2 mg). Column chromatography (chloroform) and thin layer chromatography (cyclohexane/ethyl acetate=1/2) were used for purification.

Quellen und Nachweise

ORD-Eintrag
ord-3e58f7430a744e2ca8912320f25cd48f
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07566724B2

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