関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cyanamide | HCID 9864 | — |
| 反応物 | Iodo benzene diacetate | HCID 12217721 | — |
| 反応物 | 5-(1-Methylthioethyl)-2-pentafluoroethylpyridine | HCID 59218602 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (1-[6-[Pentafluoroethyl]pyridin-3-yl]ethyl)(methyl)-lambda4-sulfanylidenecyanamide | HCID 59218616 | 85.7% |
反応手順
To a stirred solution of the 5-(1-methylthioethyl)-2-pentafluoro-ethylpyridine (A) (0.16 g, 0.6 mmol) and cyanamide (0.025 g, 0.6 mmol) in THF (3 mL) cooled to 0° C. was added iodobenzene diacetate (0.19 g, 0.6 mmol) in one portion and the resulting mixture was stirred at 0° C. for 2 h and then at room temperature overnight. The solvent was removed in vacuo and the resulting mixture was suspended in brine-saturated NaHCO3 (9:1), which was then extracted with CH2Cl2-EtOAc (1:1, v/v) two times. The combined organic layer was dried over Na2SO4, filtered, concentrated, and dried to give 0.16 g of (1-[6-[pentafluoroethyl]pyridin-3-yl]ethyl)(methyl)-λ4-sulfanylidenecyanamide (B) as a brownish oil in 85% yield. LC-MS: mass calcd for C11H10F5N3S [M]+ 311.28. Found [M−1]+ 309.84
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08288422B2 |
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| 出典データセット | uspto-grants-2012_10 |
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| ORD ID | ord-b59b7981313e47bba95b23fd78c7274d |
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| 出典メモ | uspto-grants-2012_10 |
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