Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Amantadine → N-(Adamantan-1-yl)prop-2-enimidic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Amantadine | HCID 2130 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Acryloyl chloride | HCID 13140 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(Adamantan-1-yl)prop-2-enimidic acid | HCID 284637 | 83% |
반응 단계
1-Adamantylamine (0.76 g; 5.0 mmol) and triethylamine (0.77 ml; 5.5 mmol) were dissolved in dry THF (40 mL) on an ice bath. After dropping acryloyl chloride (0.45 ml; 5.5 mmol) onto the solution, the mixture was stirred for 4 hours. After the reaction, the precipitate was removed by filtration, and the supernatant liquid was concentrated under reduced pressure. The resulting crude product was recrystallized from chloroform to give N-(1-adamantyl)acrylamide (0.85 mg; yield: 83%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09150762B2 |
| 출처 데이터셋 | uspto-grants-2015_10 |
| ORD ID | ord-f68d3521c38c43e1b183e0ec68c0dd61 |
| 출처 메모 | uspto-grants-2015_10 |