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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230350Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/230350

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=1/33/1) and thin layer chromatography (silica gel, mobile phasze: 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
PatentnummerUS07566724B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-7723b4c09e53460f8f7402e80b234a0d
Quellennotizuspto-grants-2009_07