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6-Benzyl-N-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine → N-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Benzyl-N-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine | HCID 59840713 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine | HCID 59840682 | 83.4% |
反応手順
A mixture of 6-benzyl-N-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine (7.41 g, 18.6 mmol), methanol (300 mL), and 10% palladium on charcoal (1.0 g) was evacuated and purged with hydrogen 3 times, then hydrogenated (1 atm) at room temperature for 2 days. The mixture was filtered through a pad of Celite and the filter cake was washed with MeOH. The filtrate was concentrated in vacuo to yield a pale yellow foam (4.8 g). LC-MS: 310.4 [M+H]+
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08076345B2 |
| 出典データセット | uspto-grants-2011_12 |
| ORD ID | ord-d6179fcafc0440ad85d8521f98acba1a |
| 出典メモ | uspto-grants-2011_12 |