Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → N-cyclopentylmethyl-4-(2-propynyloxy)-3-methoxybenzamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Cyclopentanemethylamine | HCID 80153 | — |
| 반응물 | 3-Methoxy-4-(2-propynyloxy)benzoyl chloride | HCID 57445671 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-cyclopentylmethyl-4-(2-propynyloxy)-3-methoxybenzamide | HCID 57445678 | 80.8% |
반응 단계
To a mixture of 10 ml of THF and 0.3 g of 3-methoxy-4-(2-propynyloxy)benzoyl chloride were added dropwise 0.15 g of cyclopentylmethylamine and 0.16 g of triethylamine in order under ice cooling. The mixture obtained was stirred at room temperature for 4 hours. Then, ethyl acetate was added to the reaction mixture and it was filtered through Celite. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.31 g of N-cyclopentylmethyl-4-(2-propynyloxy)-3-methoxybenzamide (hereinafter, described as the compound 11 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-37742500bdce49d4a45de9a444813b7b |
| 출처 메모 | uspto-grants-2011_03 |