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HRID 463988作成日:2026年10月26日

Hydrochloric Acid → Methyl 2-[[[4-(1-carboxyethoxy)-6-methyl-1,3,5-triazin-2-yl]aminocarbonyl]aminosulfonyl]benzoate

https://huagongshe.com/reaction/463988

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物Sulphonyl diisocyanateHCID 77898—
反応物Benzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
反応物Ethyl 2-[(4-amino-6-methyl-1,3,5-triazin-2-yl)oxy]propanoateHCID 19881799—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl 2-[[[4-(1-carboxyethoxy)-6-methyl-1,3,5-triazin-2-yl]aminocarbonyl]aminosulfonyl]benzoateHCID 1364675023.8%

反応手順

Methyl 2-(isocyanatosulfonyl)benzoate (10.1 g) and 8.0 g of ethyl 2-[(4-amino-6-methyl-1,3,5-triazin-2-yl)oxy]propanoate were stirred in 80 ml of methylene chloride at ambient temperature for 18 hours. An additional 2 g of the sulfonylisocyanate was added and the reaction mixture was stirred for four more hours and then 2 g more of the sulfonylisocyanate was added. After stirring for four more hours at ambient temperature, 400 ml of water was added and the pH of this mixture was adjusted to pH 8 by the addition of 10% aqueous sodium hydroxide. The aqueous phase was separated and acidified to pH 1 with hydrochloric acid to precipitate a thick white gum. Sufficient 50% aqueous sodium hydroxide was added to achieve pH 12 and the mixture was heated on a steam bath until a clear solution resulted. The solution was again acidified with hydrochloric acid to pH 3 and the resultant cloudy solution was extracted with dichlormethane. The organic phase was dried and the solvent was removed to afford 3.7 g of the title compound as a glass.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04545808
出典データセットuspto-grants-1985_10
ORD IDord-33ed3249c4dc42189aec440957359bd9
出典メモuspto-grants-1985_10