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HRID 20092作成日:2026年10月25日

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

https://huagongshe.com/reaction/20092

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). MS197.3 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745427B2
出典データセットuspto-grants-2010_06
ORD IDord-de4c3e90dbde439ca95c89e3caad9b5e
出典メモuspto-grants-2010_06