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HRID 899890作成日:2026年10月25日

Tris(hydroxymethyl)aminomethane → Methyl 2-[(4-{3-[(3-ethoxypropyl)(4-isopropylbenzyl)amino]-3-oxopropyl}phenoxy)methyl]benzoate

https://huagongshe.com/reaction/899890

反応式

関与物質

役割名称HCID仕込み量
反応物Tris(hydroxymethyl)aminomethaneHCID 6503—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 2-(bromomethyl)benzoateHCID 2734813—
反応物N-(3-ethoxypropyl)-3-(4-hydroxyphenyl)-N-(4-isopropylbenzyl)propanamideHCID 69120692—
溶媒AcetonitrileHCID 6342—
生成物Methyl 2-[(4-{3-[(3-ethoxypropyl)(4-isopropylbenzyl)amino]-3-oxopropyl}phenoxy)methyl]benzoateHCID 6913405864%

反応条件

温度60 °C

反応手順

N-(3-ethoxypropyl)-3-(4-hydroxyphenyl)-N-(4-isopropylbenzyl)propanamide (0.18 g, 0.47 mmol) and methyl 2-(bromomethyl)benzoate (0.12 g, 0.52 mmol) was dissolved in acetonitrile (10 ml) and potassium carbonate (131 mg, 0.95 mmol) was added. The mixture was stirred at 60° C. for three hours. Polymer-supported trisamine (0.3 eqv) was added and stirred overnight. The polymer was filtered off, solvent was removed by evaporation, addition of EtOAc (10 ml) and the organic phase was washed with three portions of water. After drying the crude (MgSO4) and the solvent had been removed by evaporation, the crude was purified by preparative HPLC (started with acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min). The product containing fractions were pooled and the acetonitrile was removed by evaporation. EtOAc (10 ml) was added and the organic phase was washed with two potions of brine and dried (MgSO4). Removing the solvent by evaporation gave 0.16 gram of methyl 2-[(4-{3-[(3-ethoxypropyl)(4-isopropylbenzyl)amino]-3-oxopropyl}phenoxy)methyl]benzoate (yield 63.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07355069B2
出典データセットuspto-grants-2008_04
ORD IDord-c706ddc2a87c438a9a6e210cc9197233
出典メモuspto-grants-2008_04