Water → N-((1-Benzylpyrrolidin-3-yl)methyl)cyclopropanamine

HRID 464965Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 464965
[H-].[Al+3].[Li+].[H-].[H-].[H-].O=[C:8]1[N:12]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:11][CH:10]([C:20]([NH:22][CH:23]2[CH2:25][CH2:24]2)=O)[CH2:9]1.O.[OH-].[Na+]>O1CCCC1>[C:14]1([CH2:13][N:12]2[CH2:8][CH2:9][CH:10]([CH2:20][NH:22][CH:23]3[CH2:25][CH2:24]3)[CH2:11]2)[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1

Komponenten

6

Versuchsvorschrift

To a suspension of 8.2 g (0.20 mole) of lithium aluminum hydride in 150 ml of dry tetrahydrofuran was added portionwise 18.0 g (70.0 mmole) of solid 5-oxo-1-(phenylmethyl)-N-cyclopropyl-3-pyrrolidinecarboxamide. When the addition was complete, the reaction mixture was stirred at room temperature for 18 hours and then at reflux for two hours. After cooling to room temperature, the mixture was treated dropwise, successively, with 8 ml of water, 8 ml of 15% aqueous sodium hydroxide and 24 ml of water, titrating the final addition to produce a granular precipitate. The solid was removed by filtration, washed with tetrahydrofuran and the filtrate evaporated in vacuo to give 16.0 g of 1-(phenylmethyl)-N-cyclopropyl-3-pyrrolidinemethanamine, as a heavy oil.

Aufarbeitung

  1. additionWhen the addition
  2. temperatureat reflux for two hours
  3. temperatureAfter cooling to room temperature
  4. additionthe mixture was treated dropwise
  5. additionaddition
  6. customto produce a granular precipitate
  7. customThe solid was removed by filtration
  8. washwashed with tetrahydrofuran
  9. customthe filtrate evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-323ac259628246409931e674eb1edcea
Quelldatensatz
uspto-grants-1985_10
Patentnummer
US04550103

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