Reaktion #3751

ord-7844fca8b36648daa76fa1325c5434bd

Reaktionsgleichung

CCCn1c(N)c(N=O)c(=O)n(CCC)c1=O
1,3-di-n-propyl-5-nitroso-6-aminouracil
[NH4+].[OH-]
ammonium hydroxide
O=S([O-])S(=O)[O-].[Na+].[Na+]
sodium dithionite
CCCn1c(N)c(N)c(=O)n(CCC)c1=O
1,3-di-n-propyl-5,6-diaminouracil
Ausbeute 64.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe aqueous mixture was extracted with chloroform (8×200 ml)
  2. 2
    Trocknendried over magnesium sulfate
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe residue was purified by flash chromatography (5/10% methanol/chloroform)
  6. 6
    Sonstigerecrystallized from 10% isopropanol in hexane
  7. 7
    Sonstigerecrystallized from 10% isopropanol

Vorschrift

The 1,3-di-n-propyl-5-nitroso-6-aminouracil (61.6 g) was suspended in 1 L of water, and the suspension was made alkaline to pH 11 with 50% ammonium hydroxide and treated with 100 g of sodium dithionite, in portions, until the purple color faded. The aqueous mixture was extracted with chloroform (8×200 ml), dried over magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography (5/10% methanol/chloroform) and recrystallized from 10% isopropanol in hexane and recrystallized from 10% isopropanol to yield 37.29 g of 1,3-di-n-propyl-5,6-diaminouracil, m.p., 127°-128° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05734052uspto-grants-1998_03