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HRID 2064428作成日:2026年10月25日

Cyanamide → (1-[6-[Pentafluoroethyl]pyridin-3-yl]ethyl)(methyl)-lambda4-sulfanylidenecyanamide

https://huagongshe.com/reaction/2064428

反応式

関与物質

役割名称HCID仕込み量
反応物CyanamideHCID 9864—
反応物Iodo benzene diacetateHCID 12217721—
反応物5-(1-Methylthioethyl)-2-pentafluoroethylpyridineHCID 59218602—
溶媒TetrahydrofuranHCID 8028—
生成物(1-[6-[Pentafluoroethyl]pyridin-3-yl]ethyl)(methyl)-lambda4-sulfanylidenecyanamideHCID 5921861685.7%

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08288422B2
出典データセットuspto-grants-2012_10
ORD IDord-b59b7981313e47bba95b23fd78c7274d
出典メモuspto-grants-2012_10