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HRID 2182013作成日:2026年10月26日

Dimethyl Sulfoxide → 1-[3-tert-butyl-1-(2-methylpyridin-5-yl)-1H-pyrazol-5-yl]-3-[4-(pyridin-4-yl-methoxy)naphthalen-1-yl]-urea

https://huagongshe.com/reaction/2182013

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物DiisopropylethylamineHCID 81531—
反応物5-(2,2,2-Trichloroethoxycarbonyl)amino-3-t-butyl-1-(2-methylpyridin-5-yl)pyrazoleHCID 12988816—
反応物4-(4-Pyridinylmethoxy)-1-naphthalenamineHCID 15908535—
溶媒Ethyl AcetateHCID 8857—
生成物1-[3-tert-butyl-1-(2-methylpyridin-5-yl)-1H-pyrazol-5-yl]-3-[4-(pyridin-4-yl-methoxy)naphthalen-1-yl]-ureaHCID 9957853—

反応手順

A solution of 5-(2,2,2-trichloroethoxycarbonyl)amino-3-t-butyl-1-(2-methylpyridin-5-yl)pyrazole (26 mmol), 1-amino-4-(pyridin-4-ylmethoxy)naphthalene (26 mmol), diisopropylethylamine (25 mmol) and DMSO (75 mL) is heated to 55-90° C. and held for 2-8 h. To this solution, ethyl acetate (100 mL) is added. The organic layer is washed with brine (4×50 mL), and dried over MgSO4. The solvent is removed under reduced pressure, and residue is crystallized from a suitable solvent such as acetonitrile (50 mL) at 0° C. The product is collected by filtration and recrystallized from a suitable solvent such as isopropanol and dried in vacuum to constant weight.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06894173B2
出典データセットuspto-grants-2005_05
ORD IDord-3c10cf856a084dd59d12842b762413cc
出典メモuspto-grants-2005_05