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HRID 1444747作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/1444747

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物(1,1'-Biphenyl)-4-carboxaldehydeHCID 76689—
反応物DiisopropylethylamineHCID 81531—
反応物Sodium AcetateHCID 517045—
反応物3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物3-(3-(Biphenyl-4-ylmethylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochlorideHCID 67338607—

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07662965B2
出典データセットuspto-grants-2010_02
ORD IDord-d43a3295814d480eb2cd3b064c639753
出典メモuspto-grants-2010_02