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HRID 2192398作成日:2026年10月27日

Picolinic acid → N-(2-Bromoethyl)pyridine-2-carboxamide

https://huagongshe.com/reaction/2192398

反応式

関与物質

役割名称HCID仕込み量
反応物Picolinic acidHCID 1018—
反応物TriethylamineHCID 8471—
反応物2-Bromoethylamine hydrobromideHCID 2774217—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-(2-Bromoethyl)pyridine-2-carboxamideHCID 1298347352.5%

反応手順

Picolinic acid (0.99 g) in dichloromethane (30 mL) was treated with triethylamine (1.27 mL) and HATU (3.6 g). The mixture was stirred for 10 minutes then a solution of 2-bromoethylamine hydrobromide (1.5 g) and triethylamine (1.27 mL) in dichloromethane (20 mL) was added. The reaction mixture was stirred for 3h. Water (50 mL) was added and the layers were separated. The organic layer was washed with water (3×50 mL), dried over magnesium sulphate and evaporated to afford the crude product which was purified by silica gel chromatography eluting with 0-100% EtOAc/dichloromethane. The relevant fractions were combined and evaporated, dissolved up in EtOAc (40 mL) and washed with saturated sodium hydrogen carbonate solution, ensuring the aqueous layer remained basic. The organic layer was dried over magnesium sulphate and evaporated to give the sub-titled compound (0.88 g) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08329729B2
出典データセットuspto-grants-2012_12
ORD IDord-b33c8ec9c2bf4e5184a3e9bb02ebd255
出典メモuspto-grants-2012_12