Reacción #1369161

ord-d76ea65ebb2e46309a868f3e34b441cc

Ecuación de reacción

O=c1[nH]cnc2ccsc12
3H-thieno[3,2-d]pyrimid-4-one
CN(C)C=O
DMF
CC(Cl)Cl
dichloroethane
O=C(Cl)C(=O)Cl
oxalyl chloride
Clc1ncnc2ccsc12
4-chlorothieno[3,2-d]pyrimidine
Rendimiento 82.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturarefluxed for 5 h
  2. 2
    Extracciónextracted with CH2Cl2

Procedimiento

To a solution of DMF (170.3 μL, 2.2 mmol) and dichloroethane (1.2 mL) at 0° C. under N2, oxalyl chloride (279.2 mg, 3.2 mmol) is added slowly and stirred for 10 min. 3H-thieno[3,2-d]pyrimid-4-one (152.2 mg, 1.0 mmol) is added and refluxed for 5 h. The reaction mixture is poured into water and extracted with CH2Cl2. The organic layer is stripped under reduced pressure to yield 4-chlorothieno[3,2-d]pyrimidine (140 mg, 82%) as a yellow solid. 1H NMR (DMSO) δ 9.05 (1H, s), 8.62 (1H, d, J=5 Hz), 7.79 (1H, d, J=5 Hz).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06455534B2uspto-grants-2002_09