Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → N-cyclohexylmethyl-3-fluoro-4-(2-propynyloxy)benzamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Cyclohexanemethylamine | HCID 76688 | — |
| 반응물 | 3-Fluoro-4-(2-propynyloxy)benzoyl chloride | HCID 57445684 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-cyclohexylmethyl-3-fluoro-4-(2-propynyloxy)benzamide | HCID 57445685 | 64.3% |
반응 단계
To a mixture of 10 ml of THF and 0.40 g of 3-fluoro-4-(2-propynyloxy)benzoyl chloride were added 0.45 g of cyclohexylmethylamine and 0.50 g of triethylamine in order at room temperature. The mixture obtained was stirred at room temperature for 1 hour. Then, ethyl acetate was added to the reaction mixture and the mixture was filtered through Celite. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.35 g of N-cyclohexylmethyl-3-fluoro-4-(2-propynyloxy)benzamide (hereinafter, described as the compound 22 of the present invention) represented by the formula:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07902400B2 |
| 출처 데이터셋 | uspto-grants-2011_03 |
| ORD ID | ord-7518b3286aba4f039c37a31571401569 |
| 출처 메모 | uspto-grants-2011_03 |