1-Pyrrolidineethanamine → 3-bromo-N-[2-(pyrrolidin-1-yl)ethyl]benzamide

HRID 9772

Reaktionsgleichung

Reaktionsgleichung von HRID 9772
[NH2:1][CH2:2][CH2:3][N:4]1[CH2:8][CH2:7][CH2:6][CH2:5]1.P(C#N)(OCC)(OCC)=O.C(N(CC)CC)C.[Br:26][C:27]1[CH:28]=[C:29]([CH:33]=[CH:34][CH:35]=1)[C:30](O)=[O:31]>CN(C)C=O.O>[Br:26][C:27]1[CH:28]=[C:29]([C:30]([NH:1][CH2:2][CH2:3][N:4]2[CH2:8][CH2:7][CH2:6][CH2:5]2)=[O:31])[CH:33]=[CH:34][CH:35]=1

Komponenten

7

Edukt 4

HCID 13441-PyrrolidineethanamineHCID 8471TriethylamineHCID 114563-Bromobenzoic acidHCID 76257Diethyl cyanophosphonate

Produkt 1

HCID 8486853-bromo-N-[2-(pyrrolidin-1-yl)ethyl]benzamideAusbeute 85,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

1-(2-Aminoethyl)pyrrolidine (4.34 g), diethyl cyanophosphate (5.57 ml) and triethylamine (10.4 ml) were added to a solution of 3-bromobenzoic acid (5.00 g) in N,N-dimethylformamide (DMF; 60 ml), and the mixture was stirred at room temperature for 16 hours. The reaction mixture was diluted with water and then extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residues were crystallized from hexane to give the title compound (6.31 g).

Aufarbeitung

  1. extractionextracted with diethyl ether
  2. dry with materialThe extract was dried over anhydrous magnesium sulfate
  3. customthe solvent was evaporated under reduced pressure
  4. customThe residues were crystallized from hexane

Quellen und Nachweise

ORD-Eintrag
ord-20bfb9c6c3334504a550ae3aff9a8c0e
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07091247B2

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