戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 535429作成日:2026年10月25日

Dicyclohexylcarbodiimide → 2-(methylamino)-N-[6-(2-phenylethynyl)-4-(trifluoromethyl)pyridin-2-yl]propanamide

https://huagongshe.com/reaction/535429

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-(2-Phenylethynyl)-4-(trifluoromethyl)pyridin-2-amineHCID 86694420—
溶媒DichloromethaneHCID 6344—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-(methylamino)-N-[6-(2-phenylethynyl)-4-(trifluoromethyl)pyridin-2-yl]propanamideHCID 71714918—

反応手順

A mixture of 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (620 mg, 3.05 mmol) and N,N′-dicyclohexylcarbodiimide (315 mg, 1.53 mmol) in DCM (4 ml) is stirred at RT for 30 minutes. This mixture is added to 6-(2-phenylethynyl)-4-(trifluoromethyl)pyridin-2-amine B3b (100 mg, 0.38 mmol) and DIPEA (73 μl; 0.42 mmol) in NMP (5 ml). After stirring for 6 days at 50° C. the reaction mixture is concentrated in vacuo and the boc-protected product purified by NP chromatography. The boc-protected product is treated with DCM:TFA (9:1, 4 ml) for 1.5 h at RT. This mixture is diluted with DCM and extracted with a saturated aqueous solution of NaHCO3. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by RP HPLC. Yield: 10.2 mg (8%). HPLC-MS: M+H=348; tR=1.46 (*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-515122b4d2094f3b84f0b55beec6f044
出典メモuspto-grants-2014_10