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HRID 1986191作成日:2026年10月25日
Sodium Carbonate → [2-(2-Chloropyrimidin-4-yl)-benzo[b]thiophen-6-ylmethyl]-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1986191
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | Triisopropyl borate | HCID 21531 | — |
| 反応物 | 2,4-Dichloropyrimidine | HCID 77531 | — |
| 反応物 | Lithium diisopropylamine | HCID 45051747 | — |
| 反応物 | HCID 68856189 | HCID 68856189 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 触媒 | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [2-(2-Chloropyrimidin-4-yl)-benzo[b]thiophen-6-ylmethyl]-carbamic acid tert-butyl ester | HCID 86625348 | 28.3% |
反応手順
Benzo[b]thiophen-6-ylmethyl-carbamic acid tert-butyl ester (3.6 g, 13.8 mmol) is dissolved in THF (100 mL) and cooled to −78° C. Triisopropylborate (8.5 mL) is added, followed by lithium diisopropylamine solution (27 mL of 2.0 M solution), and the reaction is allowed to slowly warm to room temperature over two hours. The reaction is stirred at room temperature for two hours at which time 2,4-dichloropyrimidine (4.59 g, 30.8 mmol), 1,1′-bis(diphenylphosphino)ferrocene (388 mg, 0.700 mmol), palladium (II) acetate (164 mg, 0.730 mmol) and sodium carbonate (28 mL of 2.0 N solution) are added. The reaction is heated for 20 hours at 70° C. After the reaction solution is cooled to 25° C., water (100 mL) is added. The mixture is extracted with dichloromethane and the extracts are evaporated. The resulting solid is subjected to chromatography on silica gel, eluting with EtOAc/hexanes 5-50%, to give the title compound (1.47 g, 28% yield). ES+(m/z) 376 (35Cl) and 378 (37Cl) [M+H].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07547691B2 |
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| 出典データセット | uspto-grants-2009_06 |
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| ORD ID | ord-e08a8a8ea1ef49318e0c9e06e6350068 |
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| 出典メモ | uspto-grants-2009_06 |
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