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Xanthine → 2-Thioxanthine

HRID 377185
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 377185
[NH:1]1[C:10](=[O:11])[C:9]2[NH:8][CH:7]=[N:6][C:5]=2[NH:4][C:2]1=O.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:13].[OH-].[Na+]>N1C=CC=CC=1>[NH:1]1[C:10](=[O:11])[C:9]2[NH:8][CH:7]=[N:6][C:5]=2[NH:4][C:2]1=[S:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 1188XanthineHCID 14798Sodium HydroxideHCID 14817Phosphorus sulfide (P2S5)

Produkt 1

HCID 12681852-ThioxanthineAusbeute 322,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

2.77 g (8.0 mM) of xanthine and 2.13 g (9.6 mM) of phosphorus pentasulfide were heated under reflux in 50 ml of pyridine for 7 days. At 0° C., 10.6 ml of 2N NaOH were added within 15 minutes. The solvents were evaporated in vacuo and the residue suspended (slow crystallization) in water. The solid was collected and washed, redissolved in 50 ml of 1N NaOH and 50 ml of isopropanol, treated twice with 0.3 g of charcoal, filtered neutralized with 5N HCl to pH 7. The isopropanol was distilled off with addition of water and the solid collected, washed and dried to give 2.60 g (89.7%) of crude thioxanthine, which was dissolved in 40 ml of dichloromethane and filtered through 30 g of silica gel: 1.91 g (65.9%) of 6-thioxanthine were recovered, mp 153-4° C.

Aufarbeitung

  1. customThe solvents were evaporated in vacuo
  2. custom(slow crystallization) in water
  3. customThe solid was collected
  4. washwashed
  5. dissolutionredissolved in 50 ml of 1N NaOH
  6. addition50 ml of isopropanol, treated twice with 0.3 g of charcoal
  7. filtrationfiltered
  8. distillationThe isopropanol was distilled off with addition of water
  9. customthe solid collected
  10. washwashed
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-f62b83c0179f402fa8d4219801364ec8
Quelldatensatz
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06025361

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