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HRID 535387作成日:2026年10月26日

Dicyclohexylcarbodiimide → tert-butyl-N-[1-[[5-bromo-6-(2-phenylethynyl)pyridin-2-yl]amino]-1-oxo-propan-2-yl]-N-methylcarbamate

https://huagongshe.com/reaction/535387

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物2-(((Tert-butoxy)carbonyl)(methyl)amino)propanoic acidHCID 4436857—
反応物5-Bromo-6-(2-phenylethynyl)pyridin-2-amineHCID 86694367—
溶媒DichloromethaneHCID 6344—
生成物tert-butyl-N-[1-[[5-bromo-6-(2-phenylethynyl)pyridin-2-yl]amino]-1-oxo-propan-2-yl]-N-methylcarbamateHCID 86694372—

反応手順

A mixture of 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (36 g, 177 mmol) and N,N′-dicyclohexylcarbodiimide (22.5 g, 109 mmol) in DCM (150 ml) is stirred with ice bath cooling for 30 minutes. A solution of 5-bromo-6-(2-phenylethynyl)pyridin-2-amine B2a (20 g, 73.2 mmol) in DCM (100 ml) is added. After stirring for 7 days at RT the reaction mixture is diluted with DCM and extracted with water. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by NP chromatography. Yield: 25 g (74%). HPLC-MS: M+H=458/460; tR=2.33 min (*Method—1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859541B2
出典データセットuspto-grants-2014_10
ORD IDord-d0dda53cdc214083ae398d2e611f12cf
出典メモuspto-grants-2014_10