1-Benzyl-(3R)-methylpiperazine-2-one → 1-Benzyl-3-methylpiperazine

HRID 234283

反応式

HRID 234283 の反応式
[CH2:1]([N:8]1[CH2:13][CH2:12][NH:11][C@H:10]([CH3:14])[C:9]1=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][NH:11][CH:10]([CH3:14])[CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

4

反応物 2

HCID 100131621-Benzyl-(3R)-methylpiperazine-2-oneHCID 21226445Aluminium lithium hydride

生成物 1

HCID 27275201-Benzyl-3-methylpiperazine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of 1-benzyl-3R-methylpiperazine-2-one (XX, 4.36 g), lithium aluminum hydride (LAH, 2.33 g) and THF (125 ml) is heated at reflux for 16 hr. After cooling to 20°-25°, the mixture is quenched slowly with water (2.3 ml), sodium hydroxide (10%, 3.5 ml) and water (5.7 ml). The residue is diluted with ether (100 ml) and is stirred for 1 hr. The solids are filtered and washed successively with ether, methylene chloride and ether. The combined filtrates are dried over potassium carbonate, filtered and concentrated to give 1-benzyl-(3R)-methylpiperazine (XXI), sufficiently pure to be carried on crude, NMR (CDCl3) 7.2-7.4, 3.49, 2.7-3.0, 1.95-2.1, 166, 1.3-1.7 and 1.01 δ.

後処理

  1. temperatureis heated
  2. temperatureat reflux for 16 hr
  3. temperatureAfter cooling to 20°-25°
  4. customthe mixture is quenched slowly with water (2.3 ml), sodium hydroxide (10%, 3.5 ml) and water (5.7 ml)
  5. additionThe residue is diluted with ether (100 ml)
  6. filtrationThe solids are filtered
  7. washwashed successively with ether, methylene chloride and ether
  8. dry with materialThe combined filtrates are dried over potassium carbonate
  9. filtrationfiltered
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-2398a8523c694a7981b6f368416efd52
出典データセット
uspto-grants-1997_01
特許番号
US05594140

関連ノート

読み込み中…