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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476638Generated: October 25, 2026

Potassium Carbonate → tert-butyl 4-{1-[(5-tert-butyl-1,3,4-oxadiazol-2-yl)methyl]-2,4-dioxo-6-phenyl-1,4-dihydrothieno[3,2-d]pyrimidin-3(2H)-yl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1476638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Tert-butyl-5-(chloromethyl)-1,3,4-oxadiazoleHCID 16778762—
Reactanttert-butyl 4-(2,4-dioxo-6-phenyl-1,4-dihydrothieno[3,2-d]pyrimidin-3(2H)-yl)piperidine-1-carboxylateHCID 67257815—
SolventDimethylformamideHCID 6228—
Producttert-butyl 4-{1-[(5-tert-butyl-1,3,4-oxadiazol-2-yl)methyl]-2,4-dioxo-6-phenyl-1,4-dihydrothieno[3,2-d]pyrimidin-3(2H)-yl}piperidine-1-carboxylateHCID 67258776—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of tert-butyl 4-(2,4-dioxo-6-phenyl-1,4-dihydrothieno[3,2-d]pyrimidin-3(2H)-yl)piperidine-1-carboxylate (2.565 g, compound B50) and 2-tert-butyl-5-(chloromethyl)-1,3,4-oxadiazole (1050 mg, compound D29) in dry DMF (50 ml) is added potassium carbonate (829 mg). The mixture is stirred for 3 h at 100° C. and subsequently poured into ice-cold water. After stirring for 5 min the resulting precipitate is filtered off and dried in vacuo to afford the title compound as a solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018175B2
Source datasetuspto-grants-2015_04
ORD IDord-8d6067b328d542288b645da9131d7fc4
Source noteuspto-grants-2015_04