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HRID 660730作成日:2026年10月26日
Sodium Carbonate → 5-[2-Benzyloxy-4-(1-triisopropylsilanyl-1H-pyrrol-3-yl)-phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one
https://huagongshe.com/reaction/660730
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 1-(Triisopropylsilyl)pyrrole-3-boronic acid | HCID 2763303 | — |
| 反応物 | 5-(2-Benzyloxy-4-iodophenyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one | HCID 68838643 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 生成物 | 5-[2-Benzyloxy-4-(1-triisopropylsilanyl-1H-pyrrol-3-yl)-phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one | HCID 68839429 | — |
反応手順
To a solution of 5-(2-benzyloxy-4-iodophenyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (100 mg, 0.225 mmol) in DME (5 mL) is added 1-triisopropylsilylpyrrole-3-boronic acid (120 mg, 0.450 mmol), Pd(PPh3)4 (27 mg, 0.023 mmol) and 0.5 mL of Na2CO3 (2M aqueous solution) and the mixture is heated in a microwave apparatus at 120° C. for 5 min. The mixture is concentrated under reduced pressure and the residue purified by reverse phase MPLC using a gradient of 10-50% MeCN/water as eluent to afford the title compound: (M−1)−=538.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08084448B2 |
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| 出典データセット | uspto-grants-2011_12 |
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| ORD ID | ord-5af0f2be0f7847ddb8a0b6853568e1d2 |
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| 出典メモ | uspto-grants-2011_12 |
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