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Piperazine → 1-(2-Methylpyridin-4-yl)piperazine

HRID 2232397
ノート
印刷プレビュー

反応式

HRID 2232397 の反応式
[N+]([O-])(O)=O.Cl[C:6]1[CH:11]=[CH:10][N:9]=[C:8]([CH3:12])[CH:7]=1.[NH:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1.C(=O)(O)[O-].[Na+].C(O)CCCC>O>[CH3:12][C:8]1[CH:7]=[C:6]([N:13]2[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]2)[CH:11]=[CH:10][N:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 4837PiperazineHCID 62761-PentanolHCID 516892Sodium BicarbonateHCID 678656864-Chloro-2-methylpyridine nitrate

生成物 1

HCID 167623771-(2-Methylpyridin-4-yl)piperazine収率 60.2%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 4-chloro-2-methylpyridine nitrate (5.00 g), piperazine (9.00 g), anhydrous sodium bicarbonate (6.60 g) and amyl alcohol (60 ml) was heated under reflux for 18 hours. The mixture was cooled and water was added to dissolve inorganic material. The organic layer was washed four times with brine and all the aqueous extracts were combined and extracted with ethyl acetate. The organic layers were combined, dried over sodium sulphate and evaporated. The residue was crystallised from ethyl acetate/hexane to give 1-(2-methylpyrid-4-yl)piperazine (2.80 g), m.p. 93°-94° C.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 18 hours
  3. temperatureThe mixture was cooled
  4. dissolutionto dissolve inorganic material
  5. washThe organic layer was washed four times with brine and all the aqueous extracts
  6. extractionextracted with ethyl acetate
  7. dry with materialdried over sodium sulphate
  8. customevaporated
  9. customThe residue was crystallised from ethyl acetate/hexane

出典と根拠

ORDレコード
ord-bacd9710458a40828c4143183fc73e44
出典データセット
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04788196

反応ノート

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