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HRID 1255878作成日:2026年10月27日

Hexamethyldisilazane → [2-(4-Benzyloxyphenyl)-ethyl]-pteridin-4-yl-amine

https://huagongshe.com/reaction/1255878

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethyldisilazaneHCID 13838—
反応物2-(4-Benzyloxy-phenyl)-ethylamineHCID 200957—
反応物Ammonium SulfateHCID 6097028—
反応物HCID 178518044HCID 178518044—
生成物[2-(4-Benzyloxyphenyl)-ethyl]-pteridin-4-yl-amineHCID 5100064073.8%

反応条件

温度114 °C

反応手順

To a mixture of pteridin-4-ol (282 mg, 1.9 mmol) and 2-(4-benzyloxyphenyl)-ethylamine (476 mg, 2.1 mmol) and hexamethyldisilazane (5 mL) in a 25 mL round bottom flask, equipped with reflux condenser, drying tube and magnetic stir bar, was added ammonium sulfate (100 mg, 0.76 mmol). The mixture was heated to 114° C. overnight and then the solvent was removed in vacuo. The residue was suspended in H2O and filtered. The filter cake was dissolved in CH2Cl2, dried with Na2SO4, filtered, and concentrated in vacuo to provide [2-(4-benzyloxyphenyl)-ethyl]-pteridin-4-yl-amine as a white solid (501 mg): 1H NMR (300 MHz) δ 9.01 (d, J=1.9 Hz, 1H), 8.81 (s, 1H), 8.61 (d, J=1.9 Hz, 1H), 7.49-7.29 (m, 6H), 7.25-7.15 (m, 3H), 6.96 (dd, J=6.8, 4.8 Hz, 2H), 5.06 (s, 2H), 3.93 (dd, J=13.2, 6.9 Hz, 2H), 3.00 (t, J=7.0 Hz, 2H); ESIMS m/z 358.1 ([M+H]+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08461164B2
出典データセットuspto-grants-2013_06
ORD IDord-39265cdc796e43df9855786b66e2bf2b
出典メモuspto-grants-2013_06