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HRID 20235作成日:2026年10月26日

Methylamine → Benzyl 4-[3-(methylcarbonylmethyl)-2-oxotetrahydropyrimidin-1(2H)-yl]piperidin-1-carboxylate

https://huagongshe.com/reaction/20235

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物[3-{1-[(Benzyloxy)carbonyl]piperidin-4-yl}-2-oxotetrahydropyrimidin-1(2H)-yl]acetic acidHCID 22137504—
溶媒TetrahydrofuranHCID 8028—
溶媒Tetrahydrofurane dichloromethaneHCID 21919333—
生成物Benzyl 4-[3-(methylcarbonylmethyl)-2-oxotetrahydropyrimidin-1(2H)-yl]piperidin-1-carboxylateHCID 68420143100.5%

反応手順

WSC (0.39 g) was added to a solution of [3-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxotetrahydropyrimidin-1(2H)-yl]acetic acid (0.70 g) obtained in Example 36a), a solution of methylamine in THF (1.85 mL) and HOBt (0.31 g) in THF/dichloromethane (1/1, 30 mL) and the mixture was stirred at room temperature overnight. The solvent were distilled off under reduced pressure, and the residue was diluted with ethyl acetate. The mixture was washed with an aqueous saturated sodium bicarbonate solution and saturated saline solution, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified with basic silica gel column chromatography (ethyl acetate) to obtain the title compound (0.70 g, 97%) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745623B2
出典データセットuspto-grants-2010_06
ORD IDord-b2e4d098bba64bbdb603aa0c7363737c
出典メモuspto-grants-2010_06