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HRID 38678作成日:2026年10月26日

3,5-Dimethylpyrazole → 2-Chloro-5-[(3,5-dimethyl-1H-pyrazol-1-yl)methyl]-1,3-thiazole

https://huagongshe.com/reaction/38678

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DimethylpyrazoleHCID 6210—
反応物Sodium hydrideHCID 24758—
反応物2-Chloro-5-chloromethylthiazoleHCID 2763179—
溶媒DimethylformamideHCID 6228—
生成物2-Chloro-5-[(3,5-dimethyl-1H-pyrazol-1-yl)methyl]-1,3-thiazoleHCID 3735087—

反応条件

温度50 °C

反応手順

A solution of 3,5-dimethyl-1H-pyrazole (Aldrich, 114 mg, 1.190 mmol) in DMF (5 ml) was added over NaH (Aldrich, 34.3 mg, 1.42 mmol) at 0° C. under N2 atmosphere. The mixture was stirred during 5 min and 2-chloro-5-(chloromethyl)-1,3-thiazole (AK scientific, 200 mg, 1.19 mmol) in DMF (2 ml) was added. The mixture was allowed to stir overnight. Finally, it was heated to 50° C. for 1 h. DMF was eliminated by washing with 14 ml of a mixture EtOAc/NH4Cl 1N (1:1). The organic layer was dried over Na2SO4 and the solution concentrated to dryness under vacuum, to afford a crude product which was chromatographed (silica gel cartridge, Hex/EtOAc) yielding the title compound. 1H NMR (300 MHz, CDCl3) δ ppm: 7.37 (s, 1H); 5.82 (s, 1H), 5.26 (s, 2H); 2.24 (s, 3H); 2.22 (s, 3H). [ES+MS] m/z: 228.1 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524750B2
出典データセットuspto-grants-2013_09
ORD IDord-f253babd52bc4cb6996371bb3ab806b7
出典メモuspto-grants-2013_09