Reaktion #2298620

ord-15cce0635eef40ada04ed0ce554d1916

Reaktionsgleichung

O=c1[nH]cnc2ccsc12
3H-thieno[3,2-d]pyrimid-4-one
O=c1[nH]cnc2ccsc12
3H-Thieno[3,2-d]pyrimid-4-one
BrBr
bromine
O=C([O-])O.[Na+]
sodium bicarbonate
O=c1[nH]cnc2c(Br)csc12
7-bromo-3H-thieno[3,2-d]pyrimid-4-one
Ausbeute 64.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was heated
  2. 2
    Temperaturat reflux for 8 hours
  3. 3
    FiltrationThe solid product was collected by vacuum filtration

Vorschrift

To a solution of 3H-thieno[3,2-d]pyrimid-4-one (82, 0.98 g, 6.4 mmol) in acetic acid (3.4 mL) was added a solution of bromine (1 mL) in acetic acid (3 mL). The reaction mixture was heated at reflux for 8 hours. The resulting suspension was allowed to cool to room temperature and then poured into a saturated aqueous solution of sodium bicarbonate to neutralize. The solid product was collected by vacuum filtration to give 7-bromo-3H-thieno[3,2-d]pyrimid-4-one (0.94 g, 64% yield) as a pale yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE039267E1uspto-grants-2006_09