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HRID 1045936作成日:2026年10月26日

Cesium carbonate → 2-(2-chloro-5-fluoropyridin-4-ylamino)-N-methylbenzamide

https://huagongshe.com/reaction/1045936

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2-Amino-N-methylbenzamideHCID 308072—
反応物2-Chloro-5-fluoro-4-iodopyridineHCID 24820495—
触媒palladium(II) acetateHCID 167845—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
溶媒1,4-DioxaneHCID 31275—
生成物2-(2-chloro-5-fluoropyridin-4-ylamino)-N-methylbenzamideHCID 5962013583%

反応条件

温度80 °C

反応手順

Cesium carbonate (651 mg, 2.00 mmol) was added to a mixture of 2-amino-N-methylbenzamide (150 mg, 1.00 mmol), 2-chloro-5-fluoro-4-iodopyridine (257 mg, 1.00 mmol), 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (35 mg, 0.06 mmol) and palladium(II) acetate (9 mg, 0.04 mmol) in dioxane (10 mL) under an atmosphere of nitrogen and the resulting suspension was heated at 80° C. for 24 hours. The mixture was filtered through Celite and the residue washed with CH2Cl2 (20 mL). The filtrate was evaporated and the residue was then dissolved in CH2Cl2 (40 mL) and washed sequentially with a saturated solution of NaHCO3 (25 mL), water (25 mL), and finally with a saturated solution of NaCl (25 mL). The organic layer was dried over MgSO4 and then evaporated to leave a solid. The solid was triturated in CH2Cl2 to afford 2-(2-chloro-5-fluoropyridin-4-ylamino)-N-methylbenzamide (231 mg, 83% yield); 1H NMR spectrum (300.132 MHz, d6 DMSO+d4 Acetic acid): δ 2.76 (3H, s), 7.19 (1H, m), 7.22 (1H, d), 7.50-7.58 (2H, m), 7.71 (1H, dd), 8.19 (1H, d); Mass spectrum: m/z (ESI+) (M+H)+=280.0 and 282.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569298B2
出典データセットuspto-grants-2013_10
ORD IDord-e750ef28b3f04adc9657fbdd73124de8
出典メモuspto-grants-2013_10