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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylamine | HCID 674 | — |
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | 5-(4-Trifluoromethyl-3-pyridyl)-1,2,4-oxadiazole-3-carboxylic acid | HCID 22744071 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | n,n-Dimethyl-5-(4-trifluoromethyl-3-pyridyl)-1,2,4-oxadiazole-3-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06239160B1 |
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| 출처 데이터셋 | uspto-grants-2001_05 |
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| ORD ID | ord-48ec8a8cce1e450ebd71fb5628b5c7e7 |
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| 출처 메모 | uspto-grants-2001_05 |
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