関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Tetravinylstannane | HCID 66189 | — |
| 反応物 | Lithium Chloride | HCID 433294 | — |
| 反応物 | 1-(7-Trifluoromethylsulfonyl-2-benzothiazolyl)-3-ethylurea | HCID 21985552 | — |
| 触媒 | HCID 178418476 | HCID 178418476 | — |
| 生成物 | 1-(7-Vinyl-2-benzothiazolyl)-3-ethylurea | HCID 21985602 | 24.5% |
反応手順
Similar to the synthesis of Example 203, a mixture of 1-(7-trifluoromethylsulfonyl-2-benzothiazolyl)-3-ethylurea (0.050 g, 80% pure, 0.11 mmol), lithium chloride (0.039 g, 0.92 mmol, 8.4 eq), triphenylphosphine (0.017 g, 0.066 mmol, 0.6 eq), Pd(PPh3)2Cl2 (0.009 g, 0.013 mmol, 0.12 eq), tetravinyltin (0.040 mL, 0.22 mmol, 2.0 eq), and a crystal of 2,6-di-tert-butyl-4-methylphenol was purged with nitrogen gas, and was heated at about 100° C. for about 1.5 hours. The mixture was taken up in MeOH, filtered, concentrated, and purified by HPLC and preparative TLC in ethyl acetate/heptane mixture to obtain 0.004 g (14%) of the desired compound. LC/MS 248 (M+1); LC retention time 2.96 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-1b2a9a1d73d34afbbad146c0399680cb |
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| 出典メモ | uspto-grants-2006_08 |
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