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HRID 493601作成日:2026年10月26日

Triethylamine → N-(5-Fluoropyridin-2-yl)pivalamide

https://huagongshe.com/reaction/493601

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Pivaloyl chlorideHCID 62493—
反応物Sodium BicarbonateHCID 516892—
反応物2-Amino-5-fluoropyridineHCID 2737701—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物N-(5-Fluoropyridin-2-yl)pivalamideHCID 2229323776.6%

反応手順

To a 0° C. solution of 2-amino-5-fluoropyridine (1.00 g, 8.92 mmol) and triethylamine (1.35 g, 13.4 mmol) in dichloromethane (30 mL) was added trimethylacetyl chloride (1.29 g, 10.7 mmol) and DMAP (0.11 g, 0.89 mmol). The solution was allowed to warm to room temperature. After 4 h, saturated aqueous NaHCO3 was added, the layers separated and the aqueous phase backwashed with DCM. The combined organics were dried over magnesium sulfate, filtered and concentrated and the residue purified by silica gel chromatography (5%→40% EtOAc/hexanes) to give the title compound (1.34 g). MS 197.3 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534784B2
出典データセットuspto-grants-2009_05
ORD IDord-bb8e3ed0f801405fb54792c8e3b8b9e9
出典メモuspto-grants-2009_05