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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532486Generated: October 25, 2026

Potassium Carbonate → Tert-butyl 4-(7-bromothieno[3,2-d]pyrimidin-4-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/532486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
Reactant7-Bromo-4-chlorothieno[3,2-d]pyrimidineHCID 16655266—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(7-bromothieno[3,2-d]pyrimidin-4-yloxy)piperidine-1-carboxylateHCID 68299345—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 7-bromo-4-chlorothieno[3,2-d]pyrimidine obtained in Step 1-3) of Preparation Example 1, t-butyl 4-hydroxypiperidine-1-carboxylate, K2CO3 and N,N-dimethylformamide were added, and stirred at 100° C. for 12 hours in a hermetically sealed reactor. The reaction mixture was cooled to room temperature, extracted with ethyl acetate and distilled water, and the organic layer thus obtained was washed with water and a saline solution. Subsequently, the washed organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853213B2
Source datasetuspto-grants-2014_10
ORD IDord-1c0ae44804e64961a128d75d75d5d4fa
Source noteuspto-grants-2014_10