Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2,4-Dichloro-6-methoxy-3,5-triazine → 4-Chloro-6-methoxy-N-{2-[4-(trifluoromethoxy)phenyl]ethyl}-1,3,5-triazin-2-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2,4-Dichloro-6-methoxy-3,5-triazine | HCID 19267 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-[4-(Trifluoromethoxy)phenyl]ethan-1-amine | HCID 10632040 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 4-Chloro-6-methoxy-N-{2-[4-(trifluoromethoxy)phenyl]ethyl}-1,3,5-triazin-2-amine | HCID 89619619 | 90.5% |
반응 단계
A solution of 5 g of 2,4-dichloro-6-methoxy-1,3,5-triazine in 50 ml of acetonitrile is cooled on an ice bath, 3.55 ml of DIPEA and then 5.13 g of 2-[4-(trifluoromethoxy)phenyl]ethanamine are added and the mixture is stirred for 30 minutes. The reaction mixture is partially concentrated under vacuum, an EtOAc/water mixture is added, the phases are separated by settling, the organic phase is washed with saturated NaCl solution and dried over MgSO4, and the solvent is evaporated off under vacuum. The precipitate formed during the evaporation is drained by suction, washed with EtOAc and dried. 7.89 g of the expected compound are obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09115121B2 |
| 출처 데이터셋 | uspto-grants-2015_08 |
| ORD ID | ord-db652a6b705346deb2812c9a881d2ec1 |
| 출처 메모 | uspto-grants-2015_08 |