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HRID 2372402생성일: 2026년 10월 25일

Hydrochloric Acid → 5-(2,6-difluorobenzyl)-4-methyl-4H-1,2,4-triazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2372402

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhosgeneHCID 6371—
반응물Ethyl 2-(methylamino)-2-oxoacetateHCID 3413434—
반응물2-(2,6-Difluorophenyl)acetohydrazideHCID 19907598—
용매PyridineHCID 1049—
용매TolueneHCID 1140—
용매ChloroformHCID 6212—
생성물5-(2,6-difluorobenzyl)-4-methyl-4H-1,2,4-triazole-3-carboxylic acid ethyl esterHCID 54338272—

반응 단계

18.6 g (142 mmol) of oxalic acid monomethylamide monoethyl ester are dissolved under a nitrogen atmosphere in 63 ml of trichloromethane, and 59 ml of a 20% solution of phosgene in toluene are added thereto. At a temperature of 5-10°, 9.2 ml of pyridine are added dropwise. The reaction mixture is then stirred for 2 hours at 0°, nitrogen being blown through the reaction mixture during the second hour. 17.6 g (95 mmol) of 2,6-difluorophenylacetic acid hydrazide are then added The reaction mixture is subsequently stirred for 40 minutes at room temperature, then poured onto ice-water, acidified with concentrated hydrochloric acid and extracted three times with ether. The acidic aqueous phase is rendered alkaline with concentrated ammonia solution and extracted by shaking three times with dichloromethane. The combined dichloromethane phases are washed twice with water, dried over magnesium sulphate and concentrated by evaporation. The residue is taken up in 160 ml of xylene and stirred under reflux for 9 hours. The reaction mixture is then concentrated and chromatographed over silica gel using ethyl acetate as eluant. The eluate is concentrated by evaporation and the crystalline residue is recrystallised from ethyl acetate/ether. 5-(2,6-difluorobenzyl)-4-methyl-4H-1,2,4-triazole-3-carboxylic acid ethyl ester of m.p. 127-128° is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05098922
출처 데이터셋uspto-grants-1992_03
ORD IDord-42185a891df44c6ca805bb7fb8eb3234
출처 메모uspto-grants-1992_03