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HRID 11353作成日:2026年10月27日

tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate

https://huagongshe.com/reaction/11353

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N-(4-aminobutyl)carbamateHCID 4351—
反応物TriethylamineHCID 8471—
反応物2,4-Dichloro-5,6-dimethyl-3-nitropyridineHCID 12109123—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamateHCID 1210912448%

反応手順

A solution of tert-butyl 4-aminobutylcarbamate (8.52 g, 45.24 mmol) in N,N-dimethylformamide was added to a solution of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (10.00 g, 45.24 mmol) and triethylamine (12.6 mL, 90.5 mmol) in N,N-dimethylformamide (320 mL). The reaction mixture was stirred overnight and then concentrated under reduced pressure. The residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate. The organics were combined, washed with brine and then concentrated under reduced pressure to provide a brown oily residue. This material was purified by flash chromatography (400 mL silica gel, eluting initially with 10% ethyl acetate in hexane and then increasing the gradient to 15% and then to 25%) to provide 8.1 g of tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098221B2
出典データセットuspto-grants-2006_08
ORD IDord-70c165635d014dcb99ca60dfce845323
出典メモuspto-grants-2006_08