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HRID 62527作成日:2026年10月26日

Potassium Phosphate, Tribasic → 2-(2-Chloro-5-cyanopyridin-4-ylamino)-N-methylbenzamide

https://huagongshe.com/reaction/62527

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Bis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
反応物2-Amino-N-methoxybenzamideHCID 12392707—
反応物6-Chloro-4-iodopyridine-3-carbonitrileHCID 57516912—
触媒Palladium (II) acetateHCID 4144353—
溶媒1,4-DioxaneHCID 31275—
生成物2-(2-Chloro-5-cyanopyridin-4-ylamino)-N-methylbenzamideHCID 57516913740.3%

反応条件

温度110 °C

反応手順

A mixture of 6-chloro-4-iodo-nicotinonitrile (14 g, 53.03 mmole, 1 eq), 2-amino-N-methoxy-benzamide (7.96 g, 53.03 mmole, 1 eq) and K3PO4 (28.14 g, 132.57 mmole, 2.5 eq) in 1,4-dioxane (250 mL) was degassed with N2 for 1 h. To this mixture were added Pd(OAC)2 (0.238 g, 1.06 mmole, 0.02 eq) and DPEPhos (2.28 g, 4.24 mmole, 0.08 eq). The resulting reaction mixture was degassed with N2 for another 15 min after which the resulting reaction mixture was stirred at 110° C. overnight. After completion of reaction solid material was collected by filtration, dissolved in water (500 mL), and extracted with ethyl acetate (5×200 mL). Combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure to give crude material. It was purified by column chromatography over silica gel (60-120 mesh) using 0.2% methanolic ammonia (10% ammonia in MeOH) in dichloromethane as the eluant to give the title compound as a pale yellow solid (9 g, 59%). 1H-NMR (400 MHz, DMSO-d6): δ 2.75 (d, 3H, J=4.56 Hz), 7.09 (s, 1H), 7.25-7.35 (m, 1H), 7.53-7.60 (m, 2H), 7.72 (d, 1H, J=7.48 Hz), 8.56 (s, 1H), 8.69-8.79 (brs, 1H), 10.65 (s, 1H). LC-MS calculated for C14H11ClN4O (M+H) 287.06, found 286.9.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09446034B2
出典データセットuspto-grants-2016_09
ORD IDord-13f3d4ff92934fd497c45693bab99090
出典メモuspto-grants-2016_09