참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| 반응물 | 2-(Trifluoromethyl)pyridine-4-carboxylic acid | HCID 14761447 | — |
| 반응물 | HCID 178458058 | HCID 178458058 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-Methoxy-N-methyl-2-(trifluoromethyl)isonicotinamide | HCID 86716069 | — |
반응 단계
To a suspension of 2-(trifluoromethyl)isonicotinic acid (1.03 g, 5.39 mmol), N,O-dimethylhydroxylamine hydrochloride (0.800 g, 8.20 mmol), N′(ethylcarbonimidoyl)-N,N-dimethyl-1,3-propanediamine hydrochloride (EDCI, 1.35 g, 7.04 mmol) and CH2Cl2 was added Et3N (1.90 mL, 13.7 mmol), and the mixture immediately turned to clear. After stirring at room temperature overnight, NH4Cl (aqueous) was added. The mixture was stirred vigorously for a while, and white solid was filtered off. The organic layer was separated, and the aqueous layer was extracted with CH2Cl2. The combined organic phases were washed with brine, and the aqueous layer was back extracted with CH2Cl2. The organic phase was dried (Na2SO4), filtered, concentrated, and purified by flash column chromatography (40 g silica gel column, 40-70% EtOAc in heptanes) to give the title compound as a clear oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09309222B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-235aeff638e64e1f991c0d1977caebea |
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| 출처 메모 | uspto-grants-2016_04 |
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