戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 344582作成日:2026年10月26日

Dicyclohexylcarbodiimide → N-[(4,6-dimethoxypyrimidin-2-yl)carbonyl]-2-methoxycarbonylbenzenesulfonamide

https://huagongshe.com/reaction/344582

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Benzoic acid, 2-(aminosulfonyl)-, methyl esterHCID 42546—
反応物4,6-Dimethoxypyrimidine-2-carboxylic acidHCID 4422483—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物N-[(4,6-dimethoxypyrimidin-2-yl)carbonyl]-2-methoxycarbonylbenzenesulfonamideHCID 14580647—

反応条件

温度0 °C

反応手順

2.2 g of 2-methoxycarbonylbenzenesulfonamide are added in portions at 0° C. to 2° C. to a mixture of 2.3 g of dicyclohexylcarbodiimide, 120 mg of 4-dimethylaminopyridine and 2.2 g of 4,6-dimethoxypyrimidine-2-carboxylic acid in 80 ml of absolute dichloromethane. The mixture is stirred for 0.5 hour at 0° C. and 2 hours at room temperature, and allowed to stand overnight. The urea which has precipitated is filtered off, the filtrate is concentrated in vacuo, and the residue is stirred for 0.5 hour with 100 ml of 2 N sodium carbonate solution. The aqueous phase is extracted using ether, and a pH of 2-3 is established using concentrated hydrochloric acid. The product which has precipitated is filtered off with suction and dried in vacuo. This gives 1.3 g of N-(4,6-dimethoxypyrimidin-2-yl)carbonyl]-2-methoxycarbonylbenzenesulfonamide of melting point 163°-165° C. (from ethyl acetate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05053072
出典データセットuspto-grants-1991_10
ORD IDord-0015cf6429ba4281ae343ec9520b699d
出典メモuspto-grants-1991_10