Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
tert-butyl N-(prop-2-yn-1-yl)carbamate → tert-Butyl 3-(4-{[(1-adamantylmethyl)amino]carbonyl}-5-chloropyridin-2-yl)prop-2-ynylcarbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | tert-butyl N-(prop-2-yn-1-yl)carbamate | HCID 11073648 | — |
| 반응물 | N-(1-adamantylmethyl)-5-chloro-2-iodoisonicotinamide | HCID 21906675 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | tert-Butyl 3-(4-{[(1-adamantylmethyl)amino]carbonyl}-5-chloropyridin-2-yl)prop-2-ynylcarbamate | HCID 21906674 | 74.4% |
반응 단계
A suspension of N-(1-adamantylmethyl)-5-chloro-2-iodoisonicotinamide (Example2(i)) (0.43 g) and tert-butyl prop-2-ynylcarbamate, (0.31 g) in anhydrous acetonitrile (5 ml) and triethylamine (5 ml) was purged with nitrogen for 5 minutes and the copper (I) iodide (0.004 g) and bis-triphenyphosphine palladium dichloride (0.014 g) were added. The mixture was stirred under nitrogen for 0.75 hours. The mixture was concentrated and the residue was purified by chromatography on silica gel eluting with acetone:dichloromethane (1:19) to afford the sub-titled compound (0.34 g) as a yellow foam.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07129246B2 |
| 출처 데이터셋 | uspto-grants-2006_10 |
| ORD ID | ord-8bab744f2d184a70b0f0f08a29c1889c |
| 출처 메모 | uspto-grants-2006_10 |