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HRID 1455249作成日:2026年10月26日

1-Hydroxybenzotriazole → 3-[2-(2-Methylsulfanyl-pyrimidine-4-carbonyl)-pyrazolidin-1-yl]-3-oxo-propionic acid ethyl ester

https://huagongshe.com/reaction/1455249

反応式

関与物質

役割名称HCID仕込み量
反応物1-HydroxybenzotriazoleHCID 75771—
反応物2-(Methylsulfanyl)pyrimidine-4-carboxylic acidHCID 295775—
反応物Sodium BicarbonateHCID 516892—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物3-Oxo-3-pyrazolidin-1-yl propionic acid ethyl esterHCID 11715304—
溶媒DimethylformamideHCID 6228—
生成物3-[2-(2-Methylsulfanyl-pyrimidine-4-carbonyl)-pyrazolidin-1-yl]-3-oxo-propionic acid ethyl esterHCID 57438084—

反応手順

To a solution of the 3-oxo-3-pyrazolidin-1-yl propionic acid ethyl ester, 11, (8.8 g, 47.7 mmol) in DMF (165 mL) is added 2-methylsulfanyl-pyrimidine-4-carboxylic acid (8.5 g, 50.1 mmol), followed by 1-hydroxybenzotriazole (12.9 g, 95.5 mmol) and then 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (11.0 g, 57.3 mmol). The reaction mixture is stirred at room temperature for 22 hours then poured into aqueous saturated NaHCO3. The aqueous phase is extracted three times with EtOAc and the combined organic phases are dried (MgSO4), filtered and concentrated in vacuo to afford 10.5 g of the desired compound which is used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07482356B2
出典データセットuspto-grants-2009_01
ORD IDord-1de3e9816c604e9bb1c03cc575f2b70e
出典メモuspto-grants-2009_01