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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 12020263 | — |
| 반응물 | Quinoline-6-carboxylic acid oxiranylmethyl ester | HCID 12020264 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | Quinoline-6-carboxylic acid 2-hydroxy-3-{3-[4-phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidin-1-yl}-propyl ester | HCID 18727469 | 83.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07135483B2 |
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| 출처 데이터셋 | uspto-grants-2006_11 |
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| ORD ID | ord-804b5ebedae54d0286a97597a6cc02aa |
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| 출처 메모 | uspto-grants-2006_11 |
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