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HRID 326710作成日:2026年10月25日

4,6-Dichloro-5-(4-methoxyphenyl)pyrimidine → N-[6-chloro-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide

https://huagongshe.com/reaction/326710

反応式

関与物質

役割名称HCID仕込み量
反応物4,6-Dichloro-5-(4-methoxyphenyl)pyrimidineHCID 19735458—
反応物p-Methoxybenzenesulfonamide potassiumHCID 67861510—
溶媒DimethylformamideHCID 6228—
生成物N-[6-chloro-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamideHCID 1973533285%

反応手順

A solution of 510 mg of 4,6-dichloro-5-(p-methoxyphenyl)pyrimidine and 680 mg of p-methoxybenzenesulfonamide potassium in 3 ml of dimethylformamide was heated at 130° C. for 1 hour. After working-up the reaction mixture, there were obtained 690 mg of N-[6-chloro-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide, melting point 165°-167° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05270313
出典データセットuspto-grants-1993_12
ORD IDord-ef826bf849a543819c621b91bbb063fc
出典メモuspto-grants-1993_12