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HRID 1365686作成日:2026年10月26日

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

https://huagongshe.com/reaction/1365686

反応式

関与物質

役割名称HCID仕込み量
反応物2-(2,6-Dichlorobenzamido)pent-4-enoic acid methyl esterHCID 57762518—
反応物(4-Acetoxybenzyl)-(4-iodophenyl)pyrimidin-2-ylamineHCID 57762581—
生成物HCID 66911977HCID 6691197766%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893046B2
出典データセットuspto-grants-2011_02
ORD IDord-100bf2a31d58464cbfe74c9014a52ad9
出典メモuspto-grants-2011_02