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HRID 1017638作成日:2026年10月25日

Citric Acid → HCID 178517354、化合物

https://huagongshe.com/reaction/1017638

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物Ammonium ChlorideHCID 25517—
反応物AzidobenzeneHCID 69319—
反応物Methyl 2-(cyanomethyl)benzoateHCID 588805—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178517354HCID 17851735464%

反応条件

温度-78 °C

反応手順

n-Butyllithium (1.6 M, 7.5 ml, 12 mmol) was added dropwise at −78° C. over 5 min to a stirred solution of methyl 2-cyanomethylbenzoate (Tetrahedron Lett., 1991, 32, 4133-4134) (2.10 g, 12 mmol) in dry THF (50 ml) under nitrogen. The deep red solution was stirred at −78° C. for 10 min, followed by the addition of a solution of phenyl azide (1.47 g, 12.3 mmol) in dry THF (10 ml). The green solution was stirred at −78° C. for 1.5 h then warmed to r.t. over 30 min, becoming bright blue. Saturated aqueous ammonium chloride (50 ml) was added and the mixture was acidified to pH 5 with 1M citric acid. The white precipitate was collected and washed with water and diethyl ether, then dried to give 3-phenyl-1,2,3-triazolo[4,5-c]isoquinolin-5-one (2.00 g, 64%). δH (360 MHz; DMSO) 7.58-7.68 (4H, m), 7.80-7.84 (2H, m), 7.93 (1H, ddd, J=8, 8 and 1), 8.30 (2H, d, J=8) and 12.80 (1H, s); m/z (ES+) 263 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479506B1
出典データセットuspto-grants-2002_11
ORD IDord-b1c8eb70268943c584ac25943102870f
出典メモuspto-grants-2002_11