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HRID 2284569作成日:2026年10月24日

Sodium Carbonate → 5-(2-Chloropyridin-3-yl)benzo[d]thiazole

https://huagongshe.com/ja/reaction/2284569

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5-BromobenzothiazoleHCID 3610155—
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1,4-DioxaneHCID 31275—
生成物5-(2-Chloropyridin-3-yl)benzo[d]thiazoleHCID 8671547770%

反応手順

5-(2-chloropyridin-3-yl)benzo[d]thiazole was prepared in the similar manner of 6-(2-chloropyridin-3-yl)benzo[d]thiazole by heating the mixture of 5-bromobenzothiazole (1.0 g, 4.67 mmol), 2-chloro-3-pyridine boronic acid pinacol ester (1.34 g, 5.6 mmol), Pd(PPh3)4 (250 mg, 0.22 mmol) and 2M aq.Na2CO3 (7 mL, 14 mmol) in 1,4-dioxane (50 mL). Upon work-up and purification protocol used in the preparation of 6-(2-chloropyridin-3-yl)benzo[d]thiazole provided 5-(2-chloropyridin-3-yl)benzo[d]thiazole as a white solid (820 mg, 70%). 1H NMR (DMSO-d6): δ 9.46 (s, 1H), 8.45 (dd, 1H, J=2.0 and 4.9 Hz), 8.27 (d, 1H, J=8.5 Hz), 8.17 (app s, 1H), 7.97 (dd, 1H, J=1.7 and 7.6 Hz), 7.58 (d, 1H, J=8.5 Hz), 7.53 (dd, 1H, J=4.7 and 7.6 Hz), LCMS: rt 6.73 min (A), purity 99%, MS (m/e) 247.

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-7cc91fbc5aa5487aa27b74c61924af06
出典メモuspto-grants-2015_09