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Water → 2-(Cyclopropylmethyl)amino-5-ethynyl pyridine

HRID 2109148
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2109148
[CH:1]1([CH2:4][NH:5][C:6]2[CH:11]=[CH:10][C:9]([C:12]#[C:13][Si](C)(C)C)=[CH:8][N:7]=2)[CH2:3][CH2:2]1.CCCC[N+](CCCC)(CCCC)CCCC.[F-].O>C1COCC1>[CH:1]1([CH2:4][NH:5][C:6]2[CH:11]=[CH:10][C:9]([C:12]#[CH:13])=[CH:8][N:7]=2)[CH2:2][CH2:3]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 2724141Tetrabutylammonium FluorideHCID 21097360Cyclopropylmethyl-(5-trimethylsilanylethynyl-pyridin-2-yl)-amine

Produkt 1

HCID 210972782-(Cyclopropylmethyl)amino-5-ethynyl pyridineAusbeute 77,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a 0° C. solution of 855 mg (3.50 mmol) of cyclopropylmethyl-(5-trimethylsilanylethynyl-pyridin-2-yl)-amine in 7 mL of THF, was slowly added 7.0 mL (7.0 mmol) of 1M TBAF in THF. The mixture was stirred for 2 h, then poured into water and extracted with Et2O. The Et2O was washed with brine. The washes were extracted once with Et2O, and the combined extracts were diluted with 10 mL of CH2Cl2 and left to sit for 10 min. The solution was then decanted from the water that had separated, and was dried with Na2SO4, filtered, concentrated, and chromatographed (1-20% EtOAc in hexanes) to provide 467 mg of 2-(cyclopropylmethyl)amino-5-ethynyl pyridine.

Aufarbeitung

  1. customTo a 0° C.
  2. extractionextracted with Et2O
  3. washThe Et2O was washed with brine
  4. extractionThe washes were extracted once with Et2O
  5. additionthe combined extracts were diluted with 10 mL of CH2Cl2
  6. waitleft
  7. waitto sit for 10 min
  8. customThe solution was then decanted from the water that
  9. customhad separated
  10. dry with materialwas dried with Na2SO4
  11. filtrationfiltered
  12. concentrationconcentrated
  13. customchromatographed (1-20% EtOAc in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-9022afb00f744d4286d92b47b7943632
Quelldatensatz
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07514458B2

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