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HRID 2196808作成日:2026年10月25日

Hydrochloric Acid → HCID 178490665、化合物

https://huagongshe.com/reaction/2196808

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-(Chloromethyl)-1,3-thiazoleHCID 2763290—
反応物Potassium tert-butoxideHCID 23665647—
反応物n-(5-Tert-butylthiazol-2-yl)-5-chloro-2-methoxybenzamideHCID 87094486—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒Ethyl AcetateHCID 8857—
溶媒tetrahydrofuran N,N-dimethylformamideHCID 21974620—
生成物HCID 178490665HCID 178490665—

反応条件

温度80 °C

反応手順

To a solution of Example 4C (0.75 g, 2.31 mmol) in N,N-dimethylformamide/tetrahydrofuran (1:4, 20 mL) were added potassium tert-butoxide (0.77 g, 6.93 mmol), tetrabutylammonium iodide (0.09, 0.23 mmol) and the commercially available HCl salt of 4-(chloromethyl)thiazole (TCI-US, 0.59 g, 3.46 mmol). The reaction mixture was stirred at 80° C. for 16 hours, cooled, diluted with ethyl acetate (20 mL) and quenched with saturated aqueous NaHCO3 (20 mL). The aqueous layer was extracted with ethyl acetate (2×20 mL). The combined organic layers were washed with water (1×25 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography using an Analogix® Intelliflash280 ™ (SiO2, 0-100% ethyl acetate in hexanes) to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 1.32 (s, 9 H), 3.76 (s, 3 H), 5.49 (s, 2 H), 7.09 (d, J=9.2 Hz, 1 H), 7.36 (s, 1 H), 7.44 (dd, J=9.0, 2.9 Hz, 1 H), 7.57 (d, J=2.0 Hz, 1 H), 7.61 (d, J=3.1 Hz, 1 H), 9.10 (d, J=2.0 Hz, 1 H); MS (ESI) m/z 422 (M+H)+; Anal. Calculated for C19H20ClN3O2S2: C, 54.08; H, 4.78; N, 9.96. Found: C, 54.10; H, 4.62; N, 9.81.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08338467B2
出典データセットuspto-grants-2012_12
ORD IDord-f4712da9c94742c3a5c53e2febb72674
出典メモuspto-grants-2012_12