Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-Methylbenzylamine → 3-(N-benzyl-N-methylamino)methyl-5-cyanomethyl-1,2,4-oxadiazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-Methylbenzylamine | HCID 7669 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-(3-Amino-1,2,4-oxadiazol-5-yl)-1-azabicyclo(2.2.1)heptane | HCID 163938 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(N-benzyl-N-methylamino)methyl-5-cyanomethyl-1,2,4-oxadiazole | HCID 20161221 | 51.7% |
반응 단계
A stirred solution of 8.0 g of the oxadiazole prepared above, 9.26 g of N-methylbenzylamine and 10.32 g of triethylamine in 50 ml of THF was allowed to stand at room temperature overnight. The reaction mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate. The resultant solution was washed with water, dried and evaporated in vacuo. The residue was chromatographed on silica gel using benzeneethyl acetate (2:1) as eluent to give 5.56 g of 3-(N-benzyl-N-methylamino)methyl-5-cyanomethyl-1,2,4-oxadiazole as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04705786 |
| 출처 데이터셋 | uspto-grants-1987_11 |
| ORD ID | ord-d472f0b3857543bf941249551c0b37ea |
| 출처 메모 | uspto-grants-1987_11 |