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Triethylamine → HCID 178418609, Verbindung

HRID 6527
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 6527
I[N:2]1[C:7]([OH:8])=[C:6]2[CH:9]=[C:10]([NH:12][C:13](=[O:18])[C:14]([CH3:17])([CH3:16])[CH3:15])[N:11]=[C:5]2[N:4]=[CH:3]1.[CH2:19]([O:22][CH:23]1[CH2:28][CH2:27][CH2:26][CH2:25][O:24]1)[C:20]#[CH:21].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(N(CC)CC)C>[Pd](Cl)Cl.C(#N)C>[O:24]1[CH2:25][CH2:26][CH2:27][CH2:28][CH:23]1[O:22][CH2:19][C:20]#[C:21][N:2]1[C:7]([OH:8])=[C:6]2[CH:9]=[C:10]([NH:12][C:13](=[O:18])[C:14]([CH3:17])([CH3:16])[CH3:15])[N:11]=[C:5]2[N:4]=[CH:3]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 8471TriethylamineHCID 11776TriphenylphosphineHCID 98609Tetrahydro-2-(2-propynyloxy)-2H-pyran2×HCID 178418587HCID 178418587, Verbindung

Produkt 1

HCID 178418609HCID 178418609, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24290
Palladium Chloride
Katalysator
HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

A mixture of 14.6 g of 3-iodo-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine, 7.6 g of 2-(2-propynyloxy)-tetrahydropyran, 798 mg (10%) of palladium chloride, 2.36 g (20%) of triphenyl phosphine, 428 mg (5%) of cuprous iodide, 45 ml of triethyl amine and 700 ml of acetonitrile is heated at reflux under nitrogen for 12 hours. There then are added to the hot reaction mixture 3.2 g of 2-(2-propynyloxy)-tetrahydropyran and reflux is continued for an additional 12 hours. After heating for a total of 24 hours under reflux, the solvent is removed under reduced pressure, and the residue filtered through silica gel using 2% methanol in methylene chloride. This filtrate is concentrated and chromatographed on silica gel eluting with 20:1 ethyl acetate:hexane mixture to give 3-(3-tetrahydropyr-2-yloxyprop-1-yn-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine which is further purified by recrystallization with ethyl acetate.

Aufarbeitung

  1. temperatureis heated
  2. temperatureat reflux under nitrogen for 12 hours
  3. temperaturereflux
  4. temperatureAfter heating for a total of 24 hours
  5. temperatureunder reflux
  6. customthe solvent is removed under reduced pressure
  7. filtrationthe residue filtered through silica gel using 2% methanol in methylene chloride
  8. concentrationThis filtrate is concentrated
  9. customchromatographed on silica gel eluting with 20:1 ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-e88b6018253240189f556b5baaee75e8
Quelldatensatz
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05248775

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