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HRID 60234作成日:2026年10月26日

Cesium carbonate → Tert-butyl (6-chloro-5-fluoropyridin-3-yl)carbamate

https://huagongshe.com/reaction/60234

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物tert-Butyl carbamateHCID 77922—
反応物5-Bromo-2-chloro-3-fluoropyridineHCID 2763285—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Tris(dibenzylideneacetone) dipalladiumHCID 9832798—
溶媒1,4-DioxaneHCID 31275—
生成物Tert-butyl (6-chloro-5-fluoropyridin-3-yl)carbamateHCID 8665604086%

反応条件

温度85 °C

反応手順

A degassed mixture of 5-bromo-2-chloro-3-fluoropyridine (22.5 g, 107 mmol), tert-butyl carbamate (13.8 g, 117.5 mmol), tris(dibenzylideneacetone) dipalladium(0) (2.95 g, 3.2 mmol), XantPhos (2.48 g, 4.28 mmol) and cesium carbonate (69.7 g, 214 mmol) in dioxane (340 mL) was heated at 85° C. for 24 hours. The reaction mixture was cooled to ambient temperature and the resultant solid was removed by filtration. The resultant solid was washed with ethyl acetate followed by dichloromethane and the filtrate was combined and concentrated in-vacuo to afford a residue that was purified by flash chromatography (silica: cyclohexane to 25% ethyl acetate/cyclohexane) to afford the title compound as a pale yellow solid (22.6 g, 86%). 1H NMR (300 MHz, CDCl3): 8.04 (dd, J=10.1, 2.4 Hz, 1H), 7.98 (d, J=2.4 Hz, 1H), 6.62 (s, 1H), 1.53 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440976B2
出典データセットuspto-grants-2016_09
ORD IDord-2aad88eff7364f1f9f9968439896e0fc
出典メモuspto-grants-2016_09