Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1444748생성일: 2026년 10월 23일
2-Fluorobiphenyl-4-carboxaldehyde → 3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride
https://huagongshe.com/ko/reaction/1444748
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Fluorobiphenyl-4-carboxaldehyde | HCID 2759083 | — |
| 반응물 | 3-(5-Ammoniopentanoyl)pyridinium chloride | HCID 67337657 | — |
| 촉매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride | HCID 67339152 | 73.8% |
반응 단계
3-(5-Ammoniopentanoyl)pyridinium chloride (150 mg, 0.60 mmol) and 2-fluorobiphenyl-4-carboxaldehyde (155 mg, 0.78 mmol) were combined in a reaction vessel and treated with ethanol (10 mL) and concentrated HCl(aq) (5 drops). The vessel was then sealed and the reaction was heated to 85° C. overnight then cooled to room temperature. The reaction mixture was then concentrated under reduced pressure then partially dissolved into hot isopropanol. This mixture was left to cool and crystals formed. The crystals were recovered by vacuum filtration, washed with fresh isopropanol, and dried under vacuum giving 92 mg (36%) of a yellow solid. LC-MS: RT=5.88 min, [M+H]+=343.1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07662965B2 |
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| 출처 데이터셋 | uspto-grants-2010_02 |
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| ORD ID | ord-7de7f797cb24449bbe4a42e5c238b9f8 |
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| 출처 메모 | uspto-grants-2010_02 |
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