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HRID 391699作成日:2026年10月25日

Sodium Azide → 1-Fluoro-2-isocyanato-4-methoxybenzene

https://huagongshe.com/reaction/391699

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium AzideHCID 33557—
反応物Oxalyl chlorideHCID 65578—
反応物2-Fluoro-5-methoxybenzoic acidHCID 2774543—
反応物HCID 57474799HCID 57474799—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒1,4-Dioxane--water (1/1)HCID 21886435—
生成物1-Fluoro-2-isocyanato-4-methoxybenzeneHCID 22150993—

反応手順

(Z)-1-(2-Amino-1,2-dicyanovinyl)-3-(2-fluoro-5-methoxyphenyl)urea. 2-Fluoro-5-methoxybenzoic acid (0.62 g, 3.62 mmol) was dissolved in CH2Cl2 (15 mL) and DMF (0.5 mL). Oxalyl chloride (0.38 mL, 4.32 mmol) was added dropwise. The mixture was stirred for another 15 min. The reaction was concentrated and then taken up in dioxane (10 mL). Sodium azide (0.26 g, 3.96 mmol) in water/dioxane (1:1 v/v, 10 mL) was added to the acid chloride at 0° C. The mixture was stirred for 10 min. The reaction was partitioned between EtOAc and water. The layers were shaken and separated. The organic layer was dried over sodium sulfate, filtered, and concentrated. The crude acyl azide was filtered through a silica gel plug (90% Hexanes in EtOAc. The filtrate was concentrated. The purified acyl azide was dissolved in toluene and stirred at 100° C. for 1 h. The toluene solution was concentrated to afford 1-fluoro-2-isocyanato-4-methoxybenzene in quantitative yield. 1-Fluoro-2-isocyanato-4-methoxybenzene (0.6 g, 3.62 mmol) was reacted with 2,3-diaminomaleonitrile (0.39 g, 3.62 mmol) according to General Procedure A to afford the title compound. MS (ESI) m/z 276.4 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383634B2
出典データセットuspto-grants-2013_02
ORD IDord-81bf7fa3d1c3454da3e25ffe2c2865cc
出典メモuspto-grants-2013_02