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HRID 524654作成日:2026年10月27日

3-Morpholinecarboxylic acid → 4-((6-(2-Bromo-4-fluorophenyl)-5-(ethoxycarbonyl)-2-(4-(2-(iso propylamino)-2-oxoethyl)thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acid

https://huagongshe.com/reaction/524654

反応式

関与物質

役割名称HCID仕込み量
反応物3-Morpholinecarboxylic acidHCID 3340152—
反応物Ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(4-(2-(isopropylamino)-2-oxo ethyl)thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 118107584—
生成物4-((6-(2-Bromo-4-fluorophenyl)-5-(ethoxycarbonyl)-2-(4-(2-(iso propylamino)-2-oxoethyl)thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acidHCID 9004329649%

反応手順

Ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(4-(2-(isopropylamino)-2-oxo ethyl)thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (1.2 g, 2 mmol) was reacted with morpholine-3-carboxylic acid (0.39 g, 3 mmol) according to the procedure as described in Example 1, Step C to give the title compound as a yellow solid (0.64 g, 49%). The compound was characterized by the following spectroscopic data:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340538B2
出典データセットuspto-grants-2016_05
ORD IDord-f6b7a4698184460fabee2b488644e3e9
出典メモuspto-grants-2016_05