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HRID 42798作成日:2026年10月25日

Nitrogen → 2-[2-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-4-ylmethyl]-4-nitro-2H-[1,2,3]triazole

https://huagongshe.com/reaction/42798

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物DiisopropylethylamineHCID 81531—
反応物4-nitro-2H-1,2,3-triazoleHCID 278150—
反応物4-Chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazoleHCID 66928813—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2-[2-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-4-ylmethyl]-4-nitro-2H-[1,2,3]triazoleHCID 67365865—

反応条件

温度50 °C

反応手順

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazole (231 mg, 1.05 mmol) in DMF (1.5 mL) was added to a solution of 4-nitro-2H-[1,2,3]triazole (100 mg, 0.88 mmol) in DMF (1.5 mL) pre-treated for 30 min with DIPEA (0.30 mL, 1.75 mmol) and the reaction mixture was stirred for 48 h at 50° C. Water (10 mL), followed by EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over NaSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (6:4 hept-EA) gave the title compound as a pale yellow oil: TLC:rf (6:4 hept-EA)=0.33. LC-MS-conditions 02: tR=0.90 min, [M+H]+=298.23.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536209B2
出典データセットuspto-grants-2013_09
ORD IDord-f88ec056013e4030b1a4a71625adc1de
出典メモuspto-grants-2013_09