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HRID 2284576作成日:2026年10月25日

Sodium Carbonate → 6-(2-Chloropyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/2284576

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物6-Bromo-[1,2,4]triazolo[1,5-a]pyridineHCID 11513934—
反応物2-Chloropyridine-3-boronic acid pinacol esterHCID 12067060—
反応物6-(2-Chloropyridin-3-yl)benzo[d]thiazoleHCID 86715476—
触媒HCID 178418397HCID 178418397—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物6-(2-Chloropyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridineHCID 8671548558%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09145433B2
出典データセットuspto-grants-2015_09
ORD IDord-c0a9d5f36e8a43eb912a492784954b0c
出典メモuspto-grants-2015_09