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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1444747생성일: 2026년 10월 26일

Hydrochloric Acid → 3-(3-(Biphenyl-4-ylmethylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride

https://huagongshe.com/reaction/1444747

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물(1,1'-Biphenyl)-4-carboxaldehydeHCID 76689—
반응물DiisopropylethylamineHCID 81531—
반응물Sodium AcetateHCID 517045—
반응물3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물3-(3-(Biphenyl-4-ylmethylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochlorideHCID 67338607—

반응 조건

온도80 °C

반응 단계

3-(5-Ammoniopentanoyl)pyridinium chloride (128 mg, 0.51 mmol) was suspended in methanol (2 mL) and treated with N,N-diisopropylethylamine (165 mg, 1.27 mmol) in a reaction vessel. This gave a clear solution. A dual solution of 0.6 M acetic acid and 0.3 M sodium acetate in methanol (10 mL) was then added, followed by addition of 4-phenylbenzaldehyde (140 mg, 0.76 mmol). The reaction vessel was then sealed and the reaction heated to 80 ° C. overnight then cooled to room temperature. The reaction mixture was then concentrated under reduced pressure, treated with a saturated solution of NaHCO3(aq), and extracted three times with EtOAc. The EtOAc extracts were washed with brine, then combined, dried over Na2SO4, filtered and concentrated under reduced pressure. The recovered material was eluted through a 20 gram column of silica gel with 7:7:7:1:0.1 hexane:MtBE:CH2Cl2:MeOH:NH4OH eluant. One sample was recovered and dried under vacuum. This sample was then dissolved into MeOH and treated with two equivalents of 6 N HCl(aq), concentrated under reduced pressure and re-crystallized from isopropanol giving 80 mg (39%) of yellow needles. LC-MS: RT=5.72 min, [M+H]+ =325.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07662965B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-d43a3295814d480eb2cd3b064c639753
출처 메모uspto-grants-2010_02