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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1365686Erstellt: 24. Oktober 2026

2-(2,6-Dichlorobenzamido)pent-4-enoic acid methyl ester → HCID 66911977, Verbindung

https://huagongshe.com/de/reaction/1365686

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(2,6-Dichlorobenzamido)pent-4-enoic acid methyl esterHCID 57762518—
Edukt(4-Acetoxybenzyl)-(4-iodophenyl)pyrimidin-2-ylamineHCID 57762581—
ProduktHCID 66911977HCID 6691197766%

Reaktionsschritte

In the same manner as in Example 1, 2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl ester (45.6 mg) was reacted with (4-iodophenyl)-(4-acetoxybenzyl)pyrimidin-2-ylamine (67.4 mg) to obtain (E)-2-(2,6-dichlorobenzamido)-5-[4-((4-acetoxy-benzyl)-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl ester (61.7 mg). Column chromatography (silica gel, eluent: ethyl acetate/hexane=1/3→3/1) and thin layer chromatography (silica gel, developing solvent: cyclohexane/ethyl acetate=1/5) were used for purification. (2) To a solution of (E)-2-(2,6-dichlorobenzamido)-5-[4-((4-acetoxy-benzyl)-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl ester (61.7 mg) in THF (3.0 ml), 0.1N aqueous sodium hydroxide solution (3.0 ml) was added, and the resulting mixture was stirred at room temperature for 2 hours. Water (50 ml) was added to the reaction solution and the resulting mixture was washed with ether. Aqueous layer was acidified by adding 1N hydrochloric acid thereto and extracted twice with ethyl acetate. Organic layers were washed with saturated brine and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated to dryness to obtain (E)-2-(2,6-dichlorobenzamido)-5-[4-((4-hydroxy-benzyl)-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid (43 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07893046B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-100bf2a31d58464cbfe74c9014a52ad9
Quellennotizuspto-grants-2011_02