Bromine → 7-Bromothieno[3,2-d]pyrimidine-2,4(1h,3h)-dione

HRID 1485485Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1485485
[NH:1]1[C:6]2[CH:7]=[CH:8][S:9][C:5]=2[C:4](=[O:10])[NH:3][C:2]1=[O:11].[Br:12]Br>C(O)(=O)C>[Br:12][C:7]1[C:6]2[NH:1][C:2](=[O:11])[NH:3][C:4](=[O:10])[C:5]=2[S:9][CH:8]=1

Komponenten

4

Edukt 2

HCID 24408BromineHCID 7059273Thieno(3,2-d)pyrimidine-2,4(1H,3H)-dione

Produkt 1

HCID 183264277-Bromothieno[3,2-d]pyrimidine-2,4(1h,3h)-dioneAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

To a solution in which thieno[3,2-d]pyrimidin-2,4(1H,3H)-dione (5.0 g, 29.5 mmol) was dissolved in glacial acetic acid (200 mL), bromine (4.55 mL, 89.0 mmol) was added. The reaction mixture solution was stirred at 110° C. for 30 hours, cooled to room temperature, and then slowly added to ice water (400 mL). Drying of thus prepared solid followed by filtration, washing several times with water and drying yielded the target compound (6.5 g, 90% yield).

Aufarbeitung

  1. temperaturecooled to room temperature
  2. customDrying of thus prepared solid
  3. filtrationfollowed by filtration
  4. washwashing several times with water
  5. customdrying

Quellen und Nachweise

ORD-Eintrag
ord-144e91a87d464feaa833501ac3017479
Quelldatensatz
uspto-grants-2016_08
Patentnummer
US09422307B2

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