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Hydrochloric Acid → HCID 178508865, Verbindung

HRID 22020
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 22020
[CH2:1](OC(OCC)CBr)[CH3:2].Cl.C([O-])(=O)C.[Na+].[NH2:16][C:17]1[N:22]=[C:21]([NH2:23])[CH:20]=[C:19]([OH:24])[N:18]=1>O>[NH2:16][C:17]1[N:18]=[C:19]([OH:24])[C:20]2[CH:2]=[CH:1][NH:23][C:21]=2[N:22]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 74852Ethane, 2-bromo-1,1-diethoxy-HCID 517045Sodium Acetate2×HCID 178507952HCID 178507952, Verbindung

Produkt 1

HCID 178508865HCID 178508865, VerbindungAusbeute 79 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

A mixture of 136.7 g of bromoacetaldehyde diethylacetal, 347 mL of water, and 17.3 mL of concentrated HCl was heated to about 90° C. with vigorous stirring for about 30 minutes, at which time a clear solution was obtained. The solution was cooled to ambient temperature and 68.3 g of sodium acetate was added. The resulting solution was added, with stirring, to a suspension of 100 g of 2,4-diamino-6-hydroxypyrimidine and 34.2 g of sodium acetate in 739 mL of water, which had been heated to 70°-85° C. The reaction was allowed to proceed for 2 hours at 70°-85° C., at which time the reaction was complete. The mixture was cooled to 0° C. and stirred for about 1.5 hours. The mixture was then filtered and the collected product was washed with 500 mL of water and 500 mL of acetone, and dried, affording 72.3 g (79%) of 2-amino-4 -hydroxy-7H-pyrrolo[2,3-d]pyrimidine, mp>300° C. NMR δ6.03 (s, 2H), 6.13 (m, 1H), 6.56 (dd, J=3.3, 2.3 Hz, 1H), 10.23 (br s, 1H), 10.93 (br s, 1H).

Aufarbeitung

  1. customwas obtained
  2. temperatureThe solution was cooled to ambient temperature
  3. additionThe resulting solution was added
  4. temperaturehad been heated to 70°-85° C
  5. waitto proceed for 2 hours at 70°-85° C., at which time
  6. temperatureThe mixture was cooled to 0° C.
  7. stirringstirred for about 1.5 hours
  8. filtrationThe mixture was then filtered
  9. washthe collected product was washed with 500 mL of water and 500 mL of acetone
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-dfede456fd9e4c148ee79d0562641559
Quelldatensatz
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05426187

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