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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 584726생성일: 2026년 10월 26일

Oxalyl chloride → 5-[1-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl]2-methylpyridine

https://huagongshe.com/reaction/584726

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물6-Methylnicotinic acidHCID 137860—
반응물2,2,2-trifluoro-N'-(4-methoxyphenyl)ethanehydrazonamideHCID 69677622—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물5-[1-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl]2-methylpyridineHCID 2234157315.3%

반응 단계

To a suspension of 6-methylnicotinoic acid (329 mg, 2.4 mmol) in dichloromethane (3 mL), was added oxalyl chloride (0.209 mL, 2.4 mmol). And then 10 micro-L of dimethylformamide was added to the mixture. The mixture was stirred for 1 hour and the solvent was removed under reduced pressure. The residue was azeotroped with dichloromethane. To the residue, was added 3 mL of dioxane. Then a solution of 2,2,2-trifluoro-N′-(4-methoxyphenyl)ethanehydrazonamide (466 mg, 2 mmol) and diisopropylethylamine (0.418 mL, 2.4 mmol) in 4.5 mL of dioxane was added to the mixture and the mixture was refluxed with stirring for 3.5 hours. The solvent was removed under reduced pressure, and dichloromethane and 0.1 N hydrochloric acid were added to the residue. The organic layer was separated, washed with 0.1 N hydrochloric acid, water, and brine, dried over magnesium sulfate. The crude product was purified by silica gel column chromatography (8:1 toluene-ethyl acetate). The desired product was rinsed with hexane and dried in vacuo to give 5-[1-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl]2-methylpyridine (102 mg, 14.8% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06927230B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-ea8c156a96844c9a98f31272410485c5
출처 메모uspto-grants-2005_08