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1,2,4-Triazolo(4,3-a)pyridin-3(2H)-one → 2-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2,4-Triazolo(4,3-a)pyridin-3(2H)-one | HCID 81431 | — |
| 反応物 | 3-(Chloromethyl)-2-(4-chlorophenyl)imidazo[1,2-a]pyridine hydrochloride | HCID 67028719 | — |
| 生成物 | 2-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one | HCID 67308637 | — |
反応手順
The title compound was prepared according to Method B and the experimentals described for compound 91 from 3-(chloromethyl)-2-(4-chlorophenyl)imidazo[1,2-a]pyridine hydrochloride and [1,2,4]triazolo[4,3-a]pyridin-3(2H)-one. M/e+ 376 for C20H15 ClN5O (M+H)+; 1H-NMR (400 MHz, CDCl3) δ 8.68 (d, J=6.9 Hz, 1H), 8.18 (d, J=8.4 Hz, 2H), 7.80 (d, J=7.3 Hz, 1H), 7.63 (d, J=9.1 Hz, 1H), 7.50 (d, J=8.4 Hz, 2H), 7.25 (m, 1H), 7.09 (dd, J=4.0, 2.9 Hz, 2H), 6.89 (m, 1H), 6.52 (m, 1H), 5.54 (s, 2H) ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08497278B2 |
| 出典データセット | uspto-grants-2013_07 |
| ORD ID | ord-6f35248635b947108261e257cd3c2f9e |
| 出典メモ | uspto-grants-2013_07 |