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HRID 247469作成日:2026年10月27日

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-(3-Chloropyridazine-6-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea

https://huagongshe.com/reaction/247469

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
反応物N-(3-chloropyridazine-6-sulfonyl)phenylcarbamateHCID 86741701—
溶媒1,4-DioxaneHCID 31275—
生成物N-(3-Chloropyridazine-6-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)ureaHCID 2127574343.3%

反応手順

A mixture of 14.2 g of N-(3-chloropyridazine-6-sulfonyl)phenylcarbamate and 6.3 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine are refluxed for 1 hour in 120 ml of absolute dioxan. When the reaction is complete, the mixture is concentrated in vacuo and the residue is taken up in a saturated aqueous solution of sodium bicarbonate and the insoluble constituents are extracted with methylene chloride. The aqueous phase is acidified with dilute hydrochloric acid and extracted with methylene chloride. The methylene chloride solution is dried over sodium sulfate and concentrated, affording 7 g of the compound of the above formula with a melting point of 135° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04707551
出典データセットuspto-grants-1987_11
ORD IDord-cc3cf87295054356b17909d3b9a248d0
出典メモuspto-grants-1987_11