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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720883생성일: 2026년 10월 26일

Piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide → Quinoline-6-carboxylic acid 2-hydroxy-3-{3-[4-phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidin-1-yl}-propyl ester

https://huagongshe.com/reaction/720883

반응식

참여 물질

역할이름HCID투입량
반응물Piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 12020263—
반응물Quinoline-6-carboxylic acid oxiranylmethyl esterHCID 12020264—
용매IsopropanolHCID 3776—
생성물Quinoline-6-carboxylic acid 2-hydroxy-3-{3-[4-phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidin-1-yl}-propyl esterHCID 1872746983.7%

반응 조건

온도70 °C

반응 단계

Piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (13) (150 mg; 0.4 mmol) is dissolved in isopropanol (10 mL) at ambient temperature. Quinoline-6-carboxylic acid oxiranylmethyl ester (17) (90.8 mg; 0.4 mmol) is added, then the mixture is heated to 70° C. and maintained for 18 hours. After cooling to ambient temperature, the solution is concentrated in vacuo at 40° C. The residue is purified via silica gel chromatography with gradient elution (1%→20% methanol in methylene chloride) affording the desired product (203.4 mg) as an oil. ESMS: MH+ 608.4 (base).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135483B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-804b5ebedae54d0286a97597a6cc02aa
출처 메모uspto-grants-2006_11