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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1978987생성일: 2026년 10월 25일

Dimethylamine → n,n-Dimethyl-5-(4-trifluoromethyl-3-pyridyl)-1,2,4-oxadiazole-3-carboxamide

https://huagongshe.com/reaction/1978987

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물5-(4-Trifluoromethyl-3-pyridyl)-1,2,4-oxadiazole-3-carboxylic acidHCID 22744071—
용매TetrahydrofuranHCID 8028—
생성물n,n-Dimethyl-5-(4-trifluoromethyl-3-pyridyl)-1,2,4-oxadiazole-3-carboxamideHCID 22744093—

반응 단계

5.8 g of carbonyidiimidazole are initially charged in 90 ml of tetrahydrofuran and, a little at a time, admixed with 9 g of 5-(4-trifluoromethyl-3-pyridyl)-1,2,4-oxadiazole-3-carboxylic acid. The mixture is stirred at room temperature for 15 min and then heated at 50° C. for 2 h. After cooling to room temperature, 2.3 g of dimethylamine are introduced in a very gentle gas stream over a period of 2 h. After a reaction time of 12 h, the mixture is concentrated and taken up in 200 ml of diethyl ether. The mixture is washed with ice-cold half conc. hydrochloric acid solution, washed neutral with sat. sodium bicarbonate sol., dried over magnesium sulfate and concentrated under reduced pressure. This gives a slightly yellow oil which solidifies after a number of days to a solid of mp. 52-54° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06239160B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-48ec8a8cce1e450ebd71fb5628b5c7e7
출처 메모uspto-grants-2001_05