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HRID 1589135作成日:2026年10月25日

Isocyanatocarbonyl chloride → 1-[4-(6-chlorobenzothiazol-2-yloxy)phenyl]-3-methyl-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione

https://huagongshe.com/reaction/1589135

反応式

関与物質

役割名称HCID仕込み量
反応物Isocyanatocarbonyl chlorideHCID 119708—
反応物N-[4-(6-chlorobenzothiazol-2-yloxy)phenyl]-N'-methylureaHCID 13506321—
溶媒1,4-DioxaneHCID 31275—
生成物1-[4-(6-chlorobenzothiazol-2-yloxy)phenyl]-3-methyl-1,3,5-triazine-2,4,6-(1H,3H,5H)-trioneHCID 1350634572.5%

反応手順

Chlorocarbonyl isocyanate (0.8 g) was added to a suspension of N-[4-(6-chlorobenzothiazol-2-yloxy)phenyl]-N'-methylurea (2.4 g) in 1,4-dioxane (50 ml), and the mixture was heated at the boiling point for 5 hours. The mixture was evaporated under reduced pressure and the residue was dissolved in a minimal volume of boiling 1,4-dioxane. After addition of ethanol (50 ml), the clear solution was cooled in a refrigerator. The resulting solid substance was collected by filtration, washed with cold ethanol and dried to give 2.1 g of 1-[4-(6-chlorobenzothiazol-2-yloxy)phenyl]-3-methyl-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione of melting point 270°-271° C. Preparation of N-[4-(6-chlorobenzothiazol-2-yloxy)phenyl]-N'-methylurea: ##STR15##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04568674
出典データセットuspto-grants-1986_02
ORD IDord-2f7093872a014b5089b7a5b08f98301b
出典メモuspto-grants-1986_02