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HRID 971187作成日:2026年10月26日

Sodium Iodide → (7-Benzyl-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidin-4-yl)-(4-trifluoromethyl-phenyl)-amine

https://huagongshe.com/reaction/971187

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物4-(Trifluoromethyl)anilineHCID 9964—
反応物Hydroiodide monohydrateHCID 21940824—
反応物7-Benzyl-4-chloro-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidineHCID 21958838—
溶媒AcetonitrileHCID 6342—
生成物(7-Benzyl-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidin-4-yl)-(4-trifluoromethyl-phenyl)-amineHCID 11246086—

反応手順

7-Benzyl-4-chloro-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine (12.0 g, 46.3 mmol) was dissolved in 20 mL of anhydrous acetonitrile and 4-(trifluoromethyl)aniline was added (7.0 mL, 55.6 mmol), followed by 47% HI/H2O (2.0 L) and sodium iodide (10.3 g, 69.5 mmol). The mixture was heated at refluxed overnight and solvents were removed under vacuum. The residue was dissolved in ethyl acetate and washed with sat. NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered and evaporated to a yellow solid which was purified by silica gel flash chromatography using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as a brown oil (15 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07312330B2
出典データセットuspto-grants-2007_12
ORD IDord-667abf842a46414db9aeab1dcda1a307
出典メモuspto-grants-2007_12