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HRID 472254作成日:2026年10月25日

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

https://huagongshe.com/reaction/472254

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EthanolHCID 702—
溶媒MethanolHCID 887—
生成物8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amineHCID 46864069—

反応手順

To a stirred suspension of hydroxylamine hydrochloride (17.4 g, 25.0 mmol) and N,N-diisopropylethylamine (26.0 mL, 14.9 mmol) in a mixture of methanol (70 mL) and ethanol (70 mL) was added N-(3-bromo-2-pyridinyl)-N′-carboethoxy-thiourea. The mixture was stirred for 2 hours at room temperature then heated to 60° C. for 18 hours. The suspension was cooled to room temperature, filtered and rinsed with methanol, water then methanol. 8-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine was isolated as an off-white solid (8.41 g, 70%). 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 8.58 (d, J=6.4 Hz, 1H), 7.73 (d, J=7.6 Hz, 1H), 6.80 (t, J=7.0 Hz, 1H), 6.25 (s, 2H). MS=213, 215 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633173B2
出典データセットuspto-grants-2014_01
ORD IDord-0155977e33124d4ab5b61c2395a3ce80
出典メモuspto-grants-2014_01