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HRID 657773作成日:2026年10月25日

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

https://huagongshe.com/reaction/657773

反応式

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-amineHCID 59840713—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物N-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amineHCID 5984068283.4%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08076345B2
出典データセットuspto-grants-2011_12
ORD IDord-d6179fcafc0440ad85d8521f98acba1a
出典メモuspto-grants-2011_12