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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67264생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물Sodium HydroxideHCID 14798—
반응물FenridazonHCID 197225—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물Dimethyl 1-(4-Chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxamideHCID 1308412149.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04345934
출처 데이터셋uspto-grants-1982_08
ORD IDord-e7436b2438204a338c6f8c00e0ebca37
출처 메모uspto-grants-1982_08