참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 3-amino-N-ethylpiperidine | HCID 98094 | — |
| 반응물 | 4-(8-Trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrate | HCID 70545502 | — |
| 촉매 | Thionyl Chloride | HCID 24386 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | N-(1-Ethyl-3-piperidyl)-4-(8-trifluoromethyl-4-quinolylamino)benzamide | HCID 20520139 | 37% |
반응 단계
11.6 Grams (0.03 mole) of 4-(8-trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrate were refluxed in thionyl chloride containing a few drops of dimethyl formamide for one hour. The thionyl chloride was evaporated and 50 milliliters of benzene were added and evaporated. The resulting acid chloride hydrochloride was added in portions with stirring to a cooled mixture of 3.84 grams (0.03 mole) of 3-amino-1-ethylpiperidine in 80 milliliters of chloroform and 31.8 grams (0.3 mole) of sodium carbonate in 100 milliliters of water. The product began to precipitate almost at once, and the mixture was stirred vigorously for two hours, and allowed to stand overnight. Filtration gave a solid which was stirred in water, collected and dried. The resulting solid was dissolved in an ethanol:chloroform mixture and chromatographed on an alumine column made up in chloroform. Elution with chloroform gave 4.9 grams (37%) of title compound as a pale yellow solid, melting point 177°-178° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04357333 |
|---|
| 출처 데이터셋 | uspto-grants-1982_11 |
|---|
| ORD ID | ord-3328dc48c13a419da6dfce9ddbcfcab7 |
|---|
| 출처 메모 | uspto-grants-1982_11 |
|---|