참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Furylacrylic acid | HCID 10876 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | HCID 86740989 | HCID 86740989 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-[beta-(2-furyl)acrylamido]-N5-methyl-N1,N1-di(n-propyl)pentane-1,5-diamide | HCID 86740990 | 80% |
반응 단계
In 75 ml of methylene chloride was dissolved 1.5 g of β-(2-furyl)acrylic acid, and 2.7 g of triethylamine and 1.3 g of ethyl chlorocarbonate were successively added thereto dropwise at -25° C. to -20° C. After 30 minutes, 3 g of the DL-2-amino-N5 -methyl-N1,N1 -di(n-propyl)-pentane-1,5-diamide hydrochloride was added to the above solution, and the resulting mixture was subjected to reaction at the same temperature for 30 minutes and at room temperature for 30 minutes. After completion of the reaction, the reaction mixture was washed successively with 30 ml of a 5% aqueous sodium hydroxide solution, 30 ml of diluted hydrochloric acid and 30 ml of water and then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure to obtain 3.1 g (yield 80%) of DL-2-[β-(2-furyl)acrylamido]-N5 -methyl-N1,N1 -di(n-propyl)pentane-1,5-diamide having a melting point of 112°-113° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04610983 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-47a1a8fa8c3e452ea1b4ee37c4296f87 |
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| 출처 메모 | uspto-grants-1986_09 |
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