戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 532486作成日:2026年10月27日

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

https://huagongshe.com/reaction/532486

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
反応物7-Bromo-4-chlorothieno[3,2-d]pyrimidineHCID 16655266—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-(7-bromothieno[3,2-d]pyrimidin-4-yloxy)piperidine-1-carboxylateHCID 68299345—

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853213B2
出典データセットuspto-grants-2014_10
ORD IDord-1c0ae44804e64961a128d75d75d5d4fa
出典メモuspto-grants-2014_10