Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
8-Methoxy-2,3,4,5,6,7-hexahydroazocine → 3-[1-(1-Benzyl-4-piperidinyl)cyclopentyl]-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-a]azocine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 8-Methoxy-2,3,4,5,6,7-hexahydroazocine | HCID 12261059 | — |
| 반응물 | 1-(1-Benzylpiperidin-4-yl)cyclopentane-1-carbohydrazide | HCID 68466971 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-[1-(1-Benzyl-4-piperidinyl)cyclopentyl]-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-a]azocine | HCID 68466809 | 50.6% |
반응 단계
1-(1-Benzylpiperidin-4-yl)cyclopentane-1-carbohydrazide (1.04 g) and 8-methoxy-2,3,4,5,6,7-hexahydroazocine (1.46 g) were reacted in toluene (10 ml) under heating to obtain 3-[1-(1-benzyl-4-piperidinyl)cyclopentyl]-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-a]azocine (0.686 g). The resulting compound was reacted in ethanol under a hydrogen atmosphere using 10% palladium-active carbon (0.14 g) as a catalyst and, after filtration through celite, the resulting solution was concentrated to obtain 3-(1-piperidin-4-ylcyclopentyl)-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-a]azocine (0.610 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07776897B2 |
| 출처 데이터셋 | uspto-grants-2010_08 |
| ORD ID | ord-2af28b3e22864275be76e364cfa3f7ba |
| 출처 메모 | uspto-grants-2010_08 |