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HRID 13810作成日:2026年10月26日

Methyl iodide → N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N-methylacetamide

https://huagongshe.com/reaction/13810

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物TetrahydrofuranHCID 8028—
反応物Cesium carbonateHCID 10796—
反応物3-acetyl-4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-1,8-naphthyridin-2(1H)-oneHCID 11260007—
生成物N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N-methylacetamideHCID 11341526—

反応手順

A solution of the product from Example 2 (60 mg) in THF (1 mL), under nitrogen, was treated with iodomethane (73 uL) and Cs2CO3 (58 mg). The suspension was stirred overnight. The reaction mixture was quenched with water and extracted with ethyl acetate. The organic layer was dried (MgSO4), filtered and concentrated in vacuo. Purification on a preparative silica TLC plate eluted with 25% EtOAc in hexane afforded the title compound. HPLC/MS: 528.1 (M+1), 530.1 (M+3); Rt=4.08 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728141B2
出典データセットuspto-grants-2010_06
ORD IDord-5eb9e7fa91e14297917b7a7df98dfbc3
出典メモuspto-grants-2010_06