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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 7-Bromo-4-chlorothieno[3,2-d]pyrimidine | HCID 16655266 | — |
| 反応物 | 4-(3-(Propan-2-yl)-1,2,4-oxadiazol-5-yl)piperidine | HCID 24208845 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 7-Bromo-4-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-1-yl]-thieno[3,2-d]pyrimidine | HCID 68299390 | 61.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08853213B2 |
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| 出典データセット | uspto-grants-2014_10 |
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| ORD ID | ord-5eb4980247e24944baaa66c8fdd70aa6 |
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| 出典メモ | uspto-grants-2014_10 |
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