反应详情

According to GP1 tert-butyl 4-(2,4-dioxo-6-phenyl-1,4-dihydrothieno[3,2-d]pyrimidin-3(2H)-yl)piperidine-1-carboxylate (6.41 g; compound B50) is reacted with 5-(chloromethyl)-3-(methoxymethyl)-1,2,4-oxadiazole (2.44 g; compound D14) in the presence of potassium carbonate (2.07 g) in DMF (45 ml). Using WU1 a solid is obtained which is dissolved in EtOAc (400 ml) at 65° C. The solvent is removed in vacuo to a volume of 40 ml at 40° C. To this solution 20 ml of diethyl ether is added at RT and the resulting suspension is filtered off and the filter cake is washed with little amounts of EtOAc and diethyl ether. The solid is dried in vacuo at 60° C. for 1 h to give the title compound.

1. customis obtained which
2. customThe solvent is removed in vacuo to a volume of 40 ml at 40° C
3. additionTo this solution 20 ml of diethyl ether is added at RT
4. filtrationthe resulting suspension is filtered off
5. washthe filter cake is washed with little amounts of EtOAc and diethyl ether
6. customThe solid is dried in vacuo at 60° C. for 1 h