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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1455249생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1455249

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물2-(Methylsulfanyl)pyrimidine-4-carboxylic acidHCID 295775—
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물3-Oxo-3-pyrazolidin-1-yl propionic acid ethyl esterHCID 11715304—
용매DimethylformamideHCID 6228—
생성물3-[2-(2-Methylsulfanyl-pyrimidine-4-carbonyl)-pyrazolidin-1-yl]-3-oxo-propionic acid ethyl esterHCID 57438084—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07482356B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-1de3e9816c604e9bb1c03cc575f2b70e
출처 메모uspto-grants-2009_01