戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 75662作成日:2026年10月26日

m-Aminoacetanilide → N-[3-[[3-Cyclopropyl-1-(2-fluoro-4-iodophenyl)-1,2,3,4,7,8-hexahydro-6,8-dimethyl-2,4,7-trioxopyrido[2,3-d]pyrimidin-5-yl]amino]phenyl]acetamide

https://huagongshe.com/reaction/75662

反応式

関与物質

役割名称HCID仕込み量
反応物m-AminoacetanilideHCID 7604—
反応物2,6-LutidineHCID 7937—
反応物DimethylacetamideHCID 31374—
反応物3-Cyclopropyl-1-(2-fluoro-4-iodophenyl)-6,8-dimethyl-5-(((4-methylphenyl)sulfonyl)oxy)pyrido(2,3-d)pyrimidine-2,4,7(1H,3H,8H)-trioneHCID 59717044—
溶媒MethanolHCID 887—
生成物N-[3-[[3-Cyclopropyl-1-(2-fluoro-4-iodophenyl)-1,2,3,4,7,8-hexahydro-6,8-dimethyl-2,4,7-trioxopyrido[2,3-d]pyrimidin-5-yl]amino]phenyl]acetamideHCID 5971735493.2%

反応条件

温度130 °C

反応手順

To p-toluenesulfonic acid 3-cyclopropyl-1-(2-fluoro-4-iodo-phenyl)-6,8-dimethyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-yl ester 77 (28.0 g) and 3′-aminoacetanilide 57 (13.2 g) were added N,N-dimethylacetamide (84.0 ml) and 2,6-lutidine (15.3 ml), and the mixture was stirred at 130° C. for 4 hrs. After allowing to cool with stirring, methanol (196 ml) was added dropwise, and the mixture was stirred at room temperature. The crystals were collected by filtration and dried to give N-{3-[3-cyclopropyl-1-(2-fluoro-4-iodo-phenyl)-6,8-dimethyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-ylamino]-phenyl}-acetamide 58 (25.2 g, yield 93%) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835443B2
出典データセットuspto-grants-2014_09
ORD IDord-bb281ffcbca54202ac961e5332aaec1a
出典メモuspto-grants-2014_09