4-Amino-5-bromo-2-chloropyrimidine → 2-Chloro-5-(2-ethoxyvinyl)pyrimidin-4-amine

HRID 1619125

Reaktionsgleichung

Reaktionsgleichung von HRID 1619125
Br[C:2]1[C:3]([NH2:9])=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1.C([Sn](CCCC)(CCCC)/[CH:15]=[CH:16]\[O:17][CH2:18][CH3:19])CCC>C1(C)C=CC=CC=1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:8][C:5]1[N:4]=[C:3]([NH2:9])[C:2](/[CH:15]=[CH:16]/[O:17][CH2:18][CH3:19])=[CH:7][N:6]=1

Komponenten

5

Versuchsvorschrift

To a degassed suspension of 5-bromo-2-chloropyrimidin-4-amine (preparation 37a, 2.50 g, 11.03 mmol) and (Z)-tributyl(2-ethoxyvinyl)stannane (4.76 g, 11.20 mmol) in toluene (40 mL) was added tetrakis(triphenylphosphine)palladium(0) (0.42 g, 0.36 mmol) and the mixture was subjected to several vacuum-argon cycles and then heated to reflux for 24 hours. Further catalyst (0.42 g, 0.36 mmol) was added and the mixture was refluxed an additional 24 hours. Further (Z)-tributyl(2-ethoxyvinyl)stannane (1.20 g, 2.82 mmol) was added and the reaction was refluxed overnight. The mixture was cooled and concentrated in vacuo and the oily residue was treated with hexanes to give a solid which was purified by flash chromatography (4:1 hexanes/ethyl acetate) to give the title compound (0.70 g, 32%) as a white solid.

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux for 24 hours
  3. temperaturethe mixture was refluxed an additional 24 hours
  4. temperaturethe reaction was refluxed overnight
  5. temperatureThe mixture was cooled
  6. concentrationconcentrated in vacuo
  7. additionthe oily residue was treated with hexanes
  8. customto give a solid which
  9. customwas purified by flash chromatography (4:1 hexanes/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-6fe11f3a56b3461eb7c32d9f2b27ffd1
Quelldatensatz
uspto-grants-2014_07
Patentnummer
US08772288B2

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