関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 6-Bromo-[1,2,4]triazolo[1,5-a]pyridine | HCID 11513934 | — |
| 反応物 | 2-Chloropyridine-3-boronic acid pinacol ester | HCID 12067060 | — |
| 反応物 | 6-(2-Chloropyridin-3-yl)benzo[d]thiazole | HCID 86715476 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 6-(2-Chloropyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridine | HCID 86715485 | 58% |
反応手順
6-(2-Chloropyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridine was synthesized in the similar to 6-(2-chloropyridin-3-yl)benzo[d]thiazole from 6-bromo[1,2,4]triazolo[1,5-a]pyridine (1.0 g, 5.0 mmol), 2-chloro-3-pyridine boronic acid pinacol ester (1.45 g, 6.0 mmol), Pd(PPh3)4 (300 mg, 0.26 mmol) and 2M aq.Na2CO3 (8 mL, 16 mmol) in 1,4-dioxane (50 mL). Upon workup, the crude residue was dissolved in CH2Cl2 (10 mL) and stirred with 50% EtOAc/hexanes (40 mL). The resulting off-white precipitate was filtered and dried to provide 6-(2-chloropyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridine (0.68 g, 58%). 1H NMR (DMSO-d6): δ 9.18 (dd, 1H, J=0.86 and 1.7 Hz), 8.57 (s, 1H), 8.50 (dd, 1H, J=1.7 and 4.9 Hz), 8.05 (dd, 1H, J=2.0 and 7.8 Hz), 7.94 (dd, 1H, J=0.9 and 9.1 Hz), 7.80 (dd, 1H, J=1.7 and 9.1 Hz), 7.59 (dd, 1H, J=4.7 and 7.6 Hz).LCMS: rt 5.00 min (A), purity 97%, MS (m/e) 231.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US09145433B2 |
|---|
| 出典データセット | uspto-grants-2015_09 |
|---|
| ORD ID | ord-c0a9d5f36e8a43eb912a492784954b0c |
|---|
| 出典メモ | uspto-grants-2015_09 |
|---|