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HRID 532474作成日:2026年10月26日

Ammonium Hydroxide → 7-Bromo-4-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-1-yl]-thieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/532474

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物DiisopropylethylamineHCID 81531—
反応物7-Bromo-4-chlorothieno[3,2-d]pyrimidineHCID 16655266—
反応物4-(3-(Propan-2-yl)-1,2,4-oxadiazol-5-yl)piperidineHCID 24208845—
溶媒IsopropanolHCID 3776—
生成物7-Bromo-4-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-1-yl]-thieno[3,2-d]pyrimidineHCID 6829939061.1%

反応条件

温度100 °C

反応手順

7-bromo-4-chlorothieno[3,2-d]pyrimidine (100 mg) was added to isopropyl alcohol (3 mL), and 4-(3-isopropyl-[1,2,4]-oxadiazol-5-yl)piperidine (100 mg) and diisopropylethylamine (200 μL) were further added thereto. The reaction mixture was stirred at 100° C. for 12 hours. Then, the reaction mixture was mixed with saturated ammonium hydroxide solution and extracted twice with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain a foamy residue. The residue was crystallized in the presence of diethyl ether to obtain the title compound (100 mg) as a whitish solid.

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-5eb4980247e24944baaa66c8fdd70aa6
出典メモuspto-grants-2014_10