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HRID 923669作成日:2026年10月26日

Dicyclohexylcarbodiimide → tert-butyl-N-methyl-N-(1-{[6-(2-phenylethynyl)-4-(pyridin-4-yl)pyridin-2-yl]-carbamoyl}ethyl)carbamate

https://huagongshe.com/reaction/923669

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物DiisopropylethylamineHCID 81531—
反応物2-(((Tert-butoxy)carbonyl)(methyl)amino)propanoic acidHCID 4436857—
反応物6-(Phenylethynyl)-[4,4'-bipyridin]-2-amineHCID 117911001—
溶媒DichloromethaneHCID 6344—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物tert-butyl-N-methyl-N-(1-{[6-(2-phenylethynyl)-4-(pyridin-4-yl)pyridin-2-yl]-carbamoyl}ethyl)carbamateHCID 117903139—

反応手順

A mixture of 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (1.44 g, 7.1 mmol) and N,N′-dicyclohexylcarbodiimide (0.73 g, 3.55 mmol) in DCM (4 ml) is stirred for 30 minutes at RT. This mixture is added in 4 portions over 48 h via syringe filter to a mixture of 6-(2-phenylethynyl)-4-(pyridin-4-yl)pyridin-2-amine G1 (0.24 g, 0.89 mmol), DIPEA (166 μl, 0.98 mmol) and NMP (2 ml) at 50° C. After stirring for another 16 h at 50° C. the mixture is filtered and the product purified by RP HPLC. Yield: 56 mg (14%). HPLC-MS: M+H=457; tR=.2.08 min (METHOD—2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09278978B2
出典データセットuspto-grants-2016_03
ORD IDord-24de4df4926842b28a6435c149caebc5
出典メモuspto-grants-2016_03