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HRID 538528作成日:2026年10月26日

Potassium Carbonate → 3-[(5-Methyl-3-pyridinyl)methoxy]benzenecarboxamide

https://huagongshe.com/reaction/538528

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物3,5-DimethylpyridineHCID 11565—
反応物N-bromobutanimideHCID 67184—
反応物3-HydroxybenzamideHCID 342403—
溶媒Carbon TetrachlorideHCID 5943—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物3-[(5-Methyl-3-pyridinyl)methoxy]benzenecarboxamideHCID 594030127.2%

反応手順

N-Bromosuccinimide (2.13 g, 12 mmol) and subsequently α,α′-azoisobutyronitrile (16 mg, 0.1 mmol) were added to a solution of 3,5-lutidine (1.14 ml, 10 mmol) in CCl4 (40 ml). The reaction mixture was stirred at reflux for 2 hrs. After cooling, succinimide was removed by filtration and the filtrate was evaporated to smaller volume (10 ml). To this filtrate, a mixture of 3-hydroxybenzenecarboxamide (550 mg, 4 mmol) and K2CO3 (830 mg, 6 mmol) in DMF (5 ml) was added and the new reaction mixture was stirred at 60° C. for 24 h. After diluting with CH2Cl2 (100 ml), the solution was washed with Na2CO3 solution (40 ml) and water (40 ml), dried (Na2SO4) and evaporated to dryness, under reduced pressure. The brown oil residue was extracted by trituration with Et2O (2×10 ml), and from the Et2O extracts, the precipitant solid was filtered and washed with pentane, to give 70 mg (7.2% yield) of the desired product. Mp 152-154° C., HPLC-MS: m/z 243 [M+H]+, Rt=2.28 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865736B2
出典データセットuspto-grants-2014_10
ORD IDord-893585267d384c23bc61c5c76b22ceee
出典メモuspto-grants-2014_10