Nitrogen → 5-isopropyl-N-methylpyridin-2-amine

HRID 594816

Reaktionsgleichung

Reaktionsgleichung von HRID 594816
[CH:1]([C:4]1[CH:5]=[CH:6][C:7]([NH2:10])=[N:8][CH:9]=1)([CH3:3])[CH3:2].N#N.[Li][CH2:14]CCC.IC>C1COCC1.O>[CH:1]([C:4]1[CH:5]=[CH:6][C:7]([NH:10][CH3:14])=[N:8][CH:9]=1)([CH3:3])[CH3:2]

Komponenten

7

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of 5-isopropyl-pyridin-2-ylamine (0.5 g, 3.67 mmol) in dry THF was purged with N2 and cooled to −78° C. n-BuLi (1.62 mL, 4.04 mmol) was added dropwise. The reaction was stirred at 0° C. for 0.5 h, and then iodomethane (0.25 mL, 4.04 mmol) was added dropwise. The resulting mixture was stirred overnight while warming to r.t. Water (20 mL) was added, and the mixture was extracted with EtOAc. The organic layer was dried over Na2SO4, concentrated, and purified by silica gel chromatography (10% to 30% EtOAc in PE) to give 200 mg (36%) of the title compound as a brown oil. [M+H] Calc'd for C9H14N2, 151. Found, 151.

Aufarbeitung

  1. additionwas added dropwise
  2. stirringThe resulting mixture was stirred overnight
  3. temperaturewhile warming to r.t
  4. extractionthe mixture was extracted with EtOAc
  5. dry with materialThe organic layer was dried over Na2SO4
  6. concentrationconcentrated
  7. custompurified by silica gel chromatography (10% to 30% EtOAc in PE)

Quellen und Nachweise

ORD-Eintrag
ord-7b88ec5d0e78410095cff08470740bd3
Quelldatensatz
uspto-grants-2016_01
Patentnummer
US09242968B2

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