Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
6-Benzyl-5,7-dihydro-5,7-dioxopyrrolo[3,4-b]pyridine → Tetrahydro-6-(phenylmethyl)-1H-pyrrolo(3,4-b)pyridine-5,7(2H,6H)-dione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 6-Benzyl-5,7-dihydro-5,7-dioxopyrrolo[3,4-b]pyridine | HCID 289502 | — |
| 촉매 | Ruthenium | HCID 23950 | — |
| 용매 | 2-Methoxyethanol | HCID 8019 | — |
| 생성물 | Tetrahydro-6-(phenylmethyl)-1H-pyrrolo(3,4-b)pyridine-5,7(2H,6H)-dione | HCID 9899604 | 101.4% |
반응 단계
To 10 g of 6-benzyl-5,7-dihydro-5,7-dioxopyrrolo[3.4-b]pyridine were added 84 ml of 2-methoxyethanol and 1.5 g of a ruthenium-on-carbon catalyst, and hydrogenation was conducted under a pressurized hydrogen gas atmosphere at 4.5 kg/cm2 for 22 hours. The catalyst was removed by filtration, and the filtrate was concentrated. To the concentrate were added 84 ml of 2-methoxyethanol and 2 g of a palladium-on-charcoal catalyst, and hydrogenation was conducted under a pressurized hydrogen gas atmosphere at 4.5 kg/cm2 for 7 hours. The catalyst was removed by filtration, and the filtrate was concentrated to yield 10.4 g of the titled compound. Throughout the hydrogenation, the reaction vessel was heated by a tungsten lamp.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05654318 |
| 출처 데이터셋 | uspto-grants-1997_08 |
| ORD ID | ord-52e932c815334e81861cd2b7329b7102 |
| 출처 메모 | uspto-grants-1997_08 |