5-(4-Nitrophenyl)-2-furaldehyde → 3-(3-((5-(4-Nitrophenyl)furan-2-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine

HRID 1444752

反応式

HRID 1444752 の反応式
[Cl-].[NH3+:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([C:9]1[CH:10]=[NH+:11][CH:12]=[CH:13][CH:14]=1)=O.[Cl-].[N+:16]([C:19]1[CH:24]=[CH:23][C:22]([C:25]2[O:31][C:28]([CH:29]=O)=[CH:27][CH:26]=2)=[CH:21][CH:20]=1)([O-:18])=[O:17]>C(O)(C)C>[N+:16]([C:19]1[CH:20]=[CH:21][C:22]([C:25]2[O:31][C:28]([CH:29]=[C:6]3[CH2:5][CH2:4][CH2:3][N:2]=[C:7]3[C:9]3[CH:10]=[N:11][CH:12]=[CH:13][CH:14]=3)=[CH:27][CH:26]=2)=[CH:23][CH:24]=1)([O-:18])=[O:17]

参加物

4

反応物 2

HCID 815675-(4-Nitrophenyl)-2-furaldehydeHCID 673376573-(5-Ammoniopentanoyl)pyridinium chloride

生成物 1

HCID 673391433-(3-((5-(4-Nitrophenyl)furan-2-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine収率 36.6%

試薬・触媒・溶媒 1

HCID 3776Isopropanol溶媒

反応条件

温度
80 °C

実験手順

3-(5-Ammoniopentanoyl)pyridinium chloride (95 mg, 0.38 mmol) and 5-(4-nitrophenyl)furfural (99 mg, 0.46 mmol) were combined in a reaction vessel and treated with isopropanol (6 mL). The reaction vessel was sealed and the reaction was heated to 80° C. with stirring overnight. The reaction was then cooled to room temperature, concentrated under reduced pressure and treated with saturated NaHCO3(aq). This mixture was then extracted three times with EtOAc. The EtOAc extracts were washed with brine, combined, dried over Na2SO4, filtered and concentrated under reduced pressure. The recovered material was eluted through a 20 gram column of silica gel with 10.5:7:7:1:0.1 hexane:MTBE:CH2Cl2:MeOH:NH4OH (1 liter). One sample was recovered that appeared to be highly crystalline. This material was re-crystallized from hot methanol. The crystals were recovered by vacuum filtration, washed with isopropanol then dried under vacuum giving 50 mg (36%) of an orange crystalline solid. LC-MS: RT=5.16 min, [M+H]+=360.0.

後処理

  1. customThe reaction vessel was sealed
  2. temperatureThe reaction was then cooled to room temperature
  3. concentrationconcentrated under reduced pressure
  4. additiontreated with saturated NaHCO3(aq)
  5. extractionThis mixture was then extracted three times with EtOAc
  6. washThe EtOAc extracts were washed with brine
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. washThe recovered material was eluted through a 20 gram column of silica gel with 10.5:7:7:1:0.1 hexane
  11. customOne sample was recovered
  12. customThis material was re-crystallized from hot methanol
  13. filtrationThe crystals were recovered by vacuum filtration
  14. washwashed with isopropanol
  15. customthen dried under vacuum

出典と根拠

ORDレコード
ord-bf7bd89e53a94d288a553d8586e3361b
出典データセット
uspto-grants-2010_02
特許番号
US07662965B2

関連ノート

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