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HRID 57763作成日:2026年10月23日

Diisopropylethylamine → 8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amine

https://huagongshe.com/ja/reaction/57763

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物Ethyl aminon-(3-bromopyridin-2-YL)methanethiocarbamateHCID 59199107—
溶媒Ethanol, mixt. with methanolHCID 18681192—
生成物8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amineHCID 4686406940,466.102%

反応条件

温度60 °C

反応手順

To a solution of hydroxylamine hydrochloride (0.10 kg, 1.4 mol, 5.0 equiv) and N,N-diisopropylethylamine (112 g, 0.867 mol, 3.00 eq) in 1:1 methanol/ethanol (1.5 L) was added ethyl [(3-bromopyridin-2-yl)carbamothioyl]carbamate (88 g, 0.29 mmol, 1 equiv) in one portion at room temperature. After 2 h, the reaction mixture was warmed to 60° C. for overnight. The reaction mixture was concentrated in vacuo, and water was added to the resulting residue. The solids were filtered and rinsed sequentially with 4:1 methanol/diethyl ether and diethyl ether to provide product as an off-white solid (25 g, 40%). LCMS (ESI) m/z: 212.8; 1H NMR (400 MHz, DMSO-d6) δ: 8.55 (m 1H), 7.70 (m, 1H), 6.75 (m, 1H), 6.20 (br s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434732B2
出典データセットuspto-grants-2016_09
ORD IDord-3745708aa5114b139119a7c422ec1767
出典メモuspto-grants-2016_09