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HRID 1044779作成日:2026年10月24日

Nitrogen → HCID 86664759、化合物

https://huagongshe.com/ja/reaction/1044779

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Sodium AzideHCID 33557—
反応物1-(4-Chloromethyl-thiazol-2-yl)ethanoneHCID 66819977—
溶媒DimethylformamideHCID 6228—
生成物HCID 86664759HCID 86664759—

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 1-(4-chloromethyl-thiazol-2-yl)-ethanone (1.08 g, 6.13 mmol) in dry DMF (21 mL) and treated with NaN3 (1.20 g, 18.39 mmol) at 65° C. until completion of the reaction. The reaction mixture was then cooled down to rt and partitioned between EA and water. The layers were separated and the org. layer dried over MgSO4, filtered and concentrated under reduced pressure to give crude 1-(4-(azidomethyl)-thiazol-2-yl)-ethanone as a yellow oil. To a solution of the crude azide (200 mg, 1.10 mmol) in THF (6 mL) were added polymer-supported Ph3P (2.0 eq.) and water (2 mL). The reaction mixture was stirred at 60° C. until completion of the reaction, cooled down to rt and filtered. The filtrate was partitioned between EA and aq. sat. NaHCO3 and the layers separated. The org. layer was dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a brown oil after purification by FC (CH2Cl2-MeOH-Et3N). LC-MS-conditions 01: tR=0.26 min; [M+H]+=157.04.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563714B2
出典データセットuspto-grants-2013_10
ORD IDord-f36e7442c31e4460b6918ebd8b5fd132
出典メモuspto-grants-2013_10