関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | (1,1'-Biphenyl)-4-carboxaldehyde | HCID 76689 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | 3-(5-Ammoniopentanoyl)pyridinium chloride | HCID 67337657 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(3-(Biphenyl-4-ylmethylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride | HCID 67338607 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07662965B2 |
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| 出典データセット | uspto-grants-2010_02 |
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| ORD ID | ord-d43a3295814d480eb2cd3b064c639753 |
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| 出典メモ | uspto-grants-2010_02 |
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