関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Boric Acid | HCID 7628 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 3-Aminophenylboric acid | HCID 21895836 | — |
| 反応物 | 1-(6-Bromo-2-benzothiazolyl)-3-ethylurea | HCID 21985564 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | N,N-Dimethylformamide--water (1/1) | HCID 21962138 | — |
| 生成物 | 1-(6-(3-Aminophenyl)-2-benzothiazolyl)-3-ethylurea | HCID 21985575 | 23.4% |
反応手順
A suspension of 1-(6-bromo-2-benzothiazolyl)-3-ethylurea (0.300 g, 1.00 mmol), 3-aminophenyl boric acid (0.237 g, 1.50 mmol, 1.5 eq), and sodium bicarbonate (0.210 g, 2.50 mmol, 2.5 eq) in 8 mL of mixed solvent DMF/water (5/1) was purged with nitrogen gas. To the mixture, the catalyst Pd(PPh3)4 (0.058 g, 0.05 mmol, 0.05 eq) was added. It was purged with nitrogen gas again, and was heated at about 100° C. in a sealed tube for about 48 hours. More Pd(PPh3)4 (0.025 g, 0.02 mmol, 0.02 eq) and more boric acid (0.080 g, 0.50 mmol, 0.50 eq) were added after the first 24 hours. The mixture was taken up in MeOH, concentrated, dissolved in methylene chloride, washed with sodium bicarbonate solution, dried (MgSO4), evaporated, and purified by flash chromatography on SiO2 with MeOH and methylene chloride (1/50) to give the desired compound 0.073 g (23%). LC/MS 313.2 (M+1); LC retention time 2.11 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091227B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-1d4c968dd1784c18a9903db176fc40d0 |
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| 出典メモ | uspto-grants-2006_08 |
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