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HRID 82329作成日:2026年10月26日

Cyanamide → (1-{6-[Chloro(difluoro)methyl]pyridin-3-yl}ethyl)(methyl)-lambda4-sulfanylidenecyanamide

https://huagongshe.com/reaction/82329

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2-[Chloro(difluoro)methyl]-5-[1-(methylthio)ethyl]pyridineHCID 59218595—
溶媒TetrahydrofuranHCID 8028—
生成物(1-{6-[Chloro(difluoro)methyl]pyridin-3-yl}ethyl)(methyl)-lambda4-sulfanylidenecyanamideHCID 2475336148%

反応手順

To a stirred solution of 2-[chloro(difluoro)methyl]-5-[1-(methylthio)-ethyl]pyridine (E) (0.32 g, 1.35 mmol) and cyanamide (0.058 g, 1.35 mmol) in THF (7 mL) was added iodobenzene diacetate (0.44 g, 1.35 mmol) in one portion at 0° C. and the resulting mixture was stirred at this temperature for 1 hr and then at room temperature for 2 hr. The solvent was then removed under reduced pressure and the resulting mixture was dissolved in CH2Cl2, washed with half-saturated brine, dried over anhydrous Na2SO4, filtered, concentrated, and purified on silica gel using 50 percent acetone in hexane to give 0.175 g of (1-{6-[chloro-(difluoro)methyl]pyridin-3-yl}ethyl)(methyl)-λ4-sulfanylidenecyanamide (F) as light-yellow oil in 48 percent yield. 1H NMR (300 MHz, CDCl3) δ 8.71 (d, J=1.8 Hz, 1H), 7.91 (dd, J=8.4, 1.8 Hz, 1H) 7.78 (d, J=8.4 Hz, 1H), 4.42 (q, J=6.9 Hz, 1H), 2.64 (s, 3H), 1.92 (d, J=6.9 Hz, 3H); LC-MS: mass calcd for C10H10ClF2N3S [M+1]+ 278. Found 278.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846717B2
出典データセットuspto-grants-2014_09
ORD IDord-51cf5689d3554ff581a9cc9cfcd8130e
出典メモuspto-grants-2014_09