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5-PyriMidinecarboxylic acid,4-[[(3-chloro-4-Methoxyphenyl)Methyl]aMino]-2-[(2S)-2-(hydroxyMethyl)-1-pyrrolidinyl]-, ethyl ester
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Product Name:
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5-PyriMidinecarboxylic acid,4-[[(3-chloro-4-Methoxyphenyl)Methyl]aMino]-2-[(2S)-2-(hydroxyMethyl)-1-pyrrolidinyl]-, ethyl ester
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Synonyms:
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5-PyriMidinecarboxylicacid,4-[[(3-chloro-4-Methoxyphenyl)Methyl]aMino]-2-[(2S)-2-(hydroxyMethyl)-1-pyrrolidinyl]-,ethylester;(S)-4-(3-chloro-4-MethoxybenzylaMino)-5-ethoxycarbonyl-2-(2-hydroxyMethyl-1-pyrrolidinyl)pyriMidine;4-[[(3-Chloro-4-methoxyphenyl)methyl]amino]-2-[(2S)-2-(hydroxymethyl)-1-pyrrolidinyl]-5-pyrimidinecarboxylicacidethylester;(S)-ethyl4-((3-chloro-4-Methoxybenzyl)aMino)-2-(2-(hydroxyMethyl)pyrrolidin-1-yl)pyriMidine-Chemicalbook5-carboxylate;ethyl(S)-4-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)pyrrolidin-1-yl)pyrimidine-5-carboxylate;5-Pyrimidinecarboxylicacid,4-[[(3-chloro-4-methoxyphenyl)methyl]amino]-2-[(2S)-2-(hydroxymethyl)-1-pyrrolidinyl]-,ethyl;(S)-Ethyl4-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)pyrrolidin-1-yl)pyrimidine-5;Ethyl4-[(3-chloro-4-methoxybenzyl)amino]-2-[(2S)-2-(hydroxymethyl)-1-pyrrolidinyl]-5-pyrimidinecarboxylate
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CAS:
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330785-83-6
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MF:
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C20H25ClN4O4
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MW:
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420.89
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EINECS
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809-849-9
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5-PyriMidinecarboxylic acid,4-[[(3-chloro-4-Methoxyphenyl)Methyl]aMino]-2-[(2S)-2-(hydroxyMethyl)-1-pyrrolidinyl]-, ethyl ester
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Density
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1.317±0.06 g/cm3 (20 ºC 760 Torr)
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Boiling point
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607.5±65.0 °C(Predicted)
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pka
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14.77±0.10(Predicted)
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Storage temp.
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2-8°C(protect from light)
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Form
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Solid
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Color
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White to off-white
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Usage
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Uses
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5-pyrimidinecarboxylic acid, 4-[[(3-chloro-4-methoxyphenyl)methyl]amino]-2-[(2S)-2-(hydroxymethyl)-1H-pyrrol-1-yl]ethyl, is a structurally complex organic compound commonly used as a key intermediate or active component in drug research and development. This compound incorporates multiple pharmacophores-including a pyrimidine ring, aromatic amine, pyrrole moiety, and hydroxymethyl group-endowing it with potential multi-target mechanisms of action, and it may be employed in the development of therapeutics for infections, cancer, inflammation, or central nervous system disorders. The (2S)-2-(hydroxymethyl)-1H-pyrrole group within its structure confers a specific stereoconfiguration, which significantly influences its biological activity and target selectivity. Meanwhile, the 3-chloro-4-methoxyphenylmethylamino side chain enhances binding affinity to biological targets. In medicinal chemistry, this compound often serves as a synthetic precursor, enabling the construction of candidate drug molecules with therapeutic potential through further structural modifications or coupling reactions, making it a vital foundational material in innovative drug development.
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