Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Trimethylsilyl cyanide → (5-fluoro-8-methoxy-4H-benzo[1,3]dioxin-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Trimethylsilyl cyanide | HCID 82115 | — |
| 반응물 | Ytterbium triflate | HCID 2733225 | — |
| 반응물 | 4-(5-Methyl-1,2,4-oxadiazol-3-yl)aniline | HCID 18188176 | — |
| 반응물 | 5-fluoro-8-methoxy-4H-benzo[1,3]dioxine-6-carbaldehyde | HCID 59516817 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (5-fluoro-8-methoxy-4H-benzo[1,3]dioxin-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrile | HCID 67097262 | — |
반응 단계
To a solution of 45 mg of Yb(OTf)3 in 3 ml of THF there were added 126 mg of 4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamine, 153 mg of 5-fluoro-8-methoxy-4H-benzo[1,3]dioxine-6-carbaldehyde, 0.2 g of MS3A and 192 μl of trimethylsilyl cyanide under a nitrogen atmosphere, and the mixture was stirred overnight at room temperature. The reaction mixture was filtered through celite, and the celite was washed with THF. The organic layer was concentrated under reduced pressure to give (5-fluoro-8-methoxy-4H-benzo[1,3]dioxin-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrile (crude product).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08163787B2 |
| 출처 데이터셋 | uspto-grants-2012_04 |
| ORD ID | ord-bbb0dc8b082c4369b261440cca9fccd0 |
| 출처 메모 | uspto-grants-2012_04 |