化工社化工社 化学情報印刷レポート · 研究参考用
Diisopropylethylamine → 8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 反応物 | Ethyl aminon-(3-bromopyridin-2-YL)methanethiocarbamate | HCID 59199107 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amine | HCID 46864069 | — |
反応手順
To a stirred suspension of hydroxylamine hydrochloride (about 17 g) and N,N-diisopropylethylamine (about 26 mL) in a mixture of methanol (about 70 mL) and ethanol (about 70 mL) is added N-(3-bromo-2-pyridinyl)-N′-carboethoxy-thiourea. The mixture is stirred for about 2 hours at room temperature then heated to about 60° C. for about 18 hours. The suspension is cooled to room temperature, filtered and rinsed with methanol, water then methanol. 8-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine is isolated as an off-white solid (about 8 g). 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09023853B2 |
| 出典データセット | uspto-grants-2015_05 |
| ORD ID | ord-94896074d91948fcb85aad83f9e7cf32 |
| 出典メモ | uspto-grants-2015_05 |