Triphenylphosphine → 6,7-Dihydro-2H-pyrano[2,3-c]pyridazin-3(5H)-one

HRID 15146

Reaktionsgleichung

Reaktionsgleichung von HRID 15146
O[CH2:2][CH2:3][CH2:4][C:5]1[C:6](=[O:12])[NH:7][NH:8][C:9](=[O:11])[CH:10]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OC(C)C)=O)=NC(OC(C)C)=O>C1COCC1>[N:7]1[NH:8][C:9](=[O:11])[CH:10]=[C:5]2[CH2:4][CH2:3][CH2:2][O:12][C:6]=12

Komponenten

5

Edukt 3

HCID 11776TriphenylphosphineHCID 75555Diisopropyl diazene-1,2-dicarboxylateHCID 675266004-(3-Hydroxypropyl)-1,2-dihydro-3,6-pyridazinedione

Produkt 1

HCID 675269516,7-Dihydro-2H-pyrano[2,3-c]pyridazin-3(5H)-oneAusbeute 79,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A suspension of 4-(3-hydroxypropyl)-1,2-dihydro-3,6-pyridazinedione (1.48 g, 8.7 mmol) in THF (105 ml) was held in an ultrasound bath for 5 minutes, then cooled under argon in an ice bath. Triphenylphosphine (3.67 g, 14 mmol) was added, followed by diisopropyl azodicarboxylate (2.76 ml, 14 mmol). After 30 minutes the solvent was evaporated and the residue kept under high vacuum overnight. Chromatography, eluting first with 2.5% methanol/dichloromethane until triphenylphosphine oxide was removed and then with 5% methanol/dichloromethane, gave the product as an off-white solid (1.049 g, 79%).

Aufarbeitung

  1. temperaturecooled under argon in an ice bath
  2. customAfter 30 minutes the solvent was evaporated
  3. customkept under high vacuum overnight
  4. washChromatography, eluting first with 2.5% methanol/dichloromethane until triphenylphosphine oxide
  5. customwas removed

Quellen und Nachweise

ORD-Eintrag
ord-742c063ba1dd404b9d9cadda52cd5a7c
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07732460B2

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