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HRID 67264作成日:2026年10月24日

Dimethylamine → Dimethyl 1-(4-Chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxamide

https://huagongshe.com/ja/reaction/67264

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物Sodium HydroxideHCID 14798—
反応物FenridazonHCID 197225—
溶媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物Dimethyl 1-(4-Chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxamideHCID 1308412149.7%

反応手順

To an ice cooled suspension of 2.65 g (0.01 mol) 1-(4-chlorophenyl)-1,4-dihydro-4-oxo-6-methyl pyridazine-3-carboxylic Acid (see Example 12) and 1.01 g (0.01 mol) of triethylamine in 50 ml of toluene there is added dropwise 1.09 g (0.01 mol) of ethyl chloroformate. The mixture is stirred at room temperature for 15 min. and is cooled to 5° C. To the mixture there is added 3.375 g (0.03 mol) of 40% dimethylamine (aqueous). The solution formed is stirred at room temperature for 18 hrs. and to it there is added 100 ml of water. The mixture is stirred at room temperature for 1 hr. and the aqueous layer is isolated. The aqueous layer is made basic with 50% sodium hydroxide and extracted with toluene. The toluene extract is dried over magnesium sulfate and concentrated in vacuo to afford 1.8 g of colorless tar. The tar is dissolved in 30 ml of methanol, saturated with anhydrous hydrogen chloride and concentrated in vacuo. The concentrate is slurried in 100 ml of ether for 1 hr. and vacuum filtered. The filter cake is air dried to afford 1.45 g (44% yield) of product, mp 125°-135° C. decomp.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04345934
出典データセットuspto-grants-1982_08
ORD IDord-e7436b2438204a338c6f8c00e0ebca37
出典メモuspto-grants-1982_08