Hydrochloric Acid → 2-Chloroadenosine

HRID 917838

Reaktionsgleichung

Reaktionsgleichung von HRID 917838
C([C@@:4]1([OH:30])[C@:8](C(=O)C)([OH:9])[C@@H:7]([CH:13](C(=O)C)[OH:14])[O:6][C@H:5]1[N:18]1[C:28]2[N:27]=[C:25](N)[NH:24][C:22](Cl)(O)[C:21]=2[N:20]=[CH:19]1)(=O)C.[N:31]([O-])=O.[Na+].[ClH:35]>O.N>[Cl:35][C:25]1[N:24]=[C:22]([NH2:31])[C:21]2[N:20]=[CH:19][N:18]([C:28]=2[N:27]=1)[C@@H:5]1[O:6][C@H:7]([CH2:13][OH:14])[C@@H:8]([OH:9])[C@H:4]1[OH:30]

Komponenten

6

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

100 g of 2',3',5'-triacetyl-6-chloroguanosine was dissolved in 400 ml of concentrated hydrochloric acid and, after the mixture was cooled to 0°C, a solution of 20 g of sodium nitrite dissolved in 50 ml of water was then added slowly to the mixture. The resulting mixture was allowed to react for 30 minutes, neutralized with concentrated aqueous ammonia and extracted with 2 l of methylene chloride. The extract was dried over anhydrous sodium sulfate and concentrated. The concentrate thus-obtained was dissolved in 300 ml of saturated methanolic ammonia and the mixture was allowed to react at a temperature of 100°C for 5 hours in a sealed tube. The reaction mixture was then concentrated to dryness and the residue was crystallized from water to obtain 42.3 g (60% yield) of 2-chloroadenosine. Recrystallization from water was repeated to obtain crystals having the following constant physical properties. Melting Point: 161° ~ 162°C (with decomposition)

Aufarbeitung

  1. additionwas then added slowly to the mixture
  2. customto react for 30 minutes
  3. extractionextracted with 2 l of methylene chloride
  4. dry with materialThe extract was dried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customThe concentrate thus-obtained
  7. customto react at a temperature of 100°C for 5 hours in a sealed tube
  8. concentrationThe reaction mixture was then concentrated to dryness
  9. customthe residue was crystallized from water

Quellen und Nachweise

ORD-Eintrag
ord-c57adab49dea4d91965af19d4b410f11
Quelldatensatz
uspto-grants-1976_07
Patentnummer
US03968102

Verknüpfte Notizen

Wird geladen…