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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22682생성일: 2026년 10월 23일

Triethylamine → 2-[2-(4-Fluorophenyl)acetyl]-4-(2,2-dimethylpropionyloxy) pyrazolidine-1-carboxylic acid 1-benzyl ester

https://huagongshe.com/ko/reaction/22682

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-(4-Fluorophenyl)acetic acidHCID 9837—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-(2,2-Dimethylpropionyloxy)pyrazolidine-1-carboxylic acid 1-benzyl esterHCID 20724748—
용매DichloromethaneHCID 6344—
생성물2-[2-(4-Fluorophenyl)acetyl]-4-(2,2-dimethylpropionyloxy) pyrazolidine-1-carboxylic acid 1-benzyl esterHCID 2072474791%

반응 조건

온도0 °C

반응 단계

4-(2,2-Dimethylpropionyloxy)-pyrazolidine-1-carboxylic acid 1-benzyl ester, 30, (1.45 g, 4.23 mmol) is dissolved in dichloromethane (21 mL). The solution is cooled to 0° C. and triethylamine (1.30 mL, 9.31 mmol) added dropwise via syringe. The cold bath is removed and the reaction allowed to warm to room temperature and continue stirring 20 minutes. 4-Fluorophenylacetic acid (848 mg, 5.50 mmol) is added. After stirring for 5 minutes, the reaction mixture is transferred via cannula into a solution of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrogen chloride in dichloromethane (21 mL) maintained at 0° C. The reaction is allowed to stir and gradually warm to room temperature over 12 hours. The reaction is washed with a 5% aqueous solution of Na2CO3 (2×50 mL). The combined aqueous layers are extracted several times with dichloromethane (50 mL) and the combined organic layers washed with brine, dried, filtered and concentrated in vacuo. The crude product is purified over silica (2:1 to 1:1 hexane/ethyl acetate) to afford 1.71 g (91% yield) of the desired product as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849627B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-21bba38f12764b9f8e18cb2a3fb78b24
출처 메모uspto-grants-2005_02