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HRID 1472878作成日:2026年10月26日
1-Benzyl-1H-pyrazole-4-boronic acid → 5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine
https://huagongshe.com/reaction/1472878
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1-Benzyl-1H-pyrazole-4-boronic acid | HCID 3352881 | — |
| 反応物 | 5-Methylsulfanyl-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine | HCID 59589529 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine | HCID 59589583 | — |
反応手順
A microwave vial containing 5-methylsulfanyl-[1,2,4]triazolo[1,5-c]pyrimidin-2-ylamine (0.05 g, 0.276 mmol), 1-benzyl-1H-pyrazole-4-boronic acid (123 mg, 0.607 mmol), copper(1)thiophene carboxylate (116 mg, 0.607 mmol) and tetrakis(triphenylphosphine)palladium (33 mg, 0.028 mmol) in THF (1.2 mL) was heated under microwave irradiation (130° C., 15 min). The reaction mixture was filtered through celite and the cake washed with dichloromethane. The filtrate was washed with water followed by brine, dried over magnesium sulfate and concentrated under vacuum. Trituration with diethyl ether provided a yellow solid that did not require further purification. Yield: 0.05 g, 63%; LCMS method: 2, RT: 3.18 min, MI: 292 [M+1].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09012633B2 |
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| 出典データセット | uspto-grants-2015_04 |
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| ORD ID | ord-6e160dad9d544c888671cea1d32f8f85 |
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| 出典メモ | uspto-grants-2015_04 |
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