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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339789생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/339789

반응식

참여 물질

역할이름HCID투입량
반응물HexamethyldisilazaneHCID 13838—
반응물2-(4-Benzyloxy-phenyl)-ethylamineHCID 200957—
반응물Ammonium SulfateHCID 6097028—
반응물HCID 178518044HCID 178518044—
생성물[2-(4-Benzyloxyphenyl)-ethyl]-pteridin-4-yl-amineHCID 5100064073.8%

반응 조건

온도114 °C

반응 단계

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]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895568B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-77c73c745c1c4686897b5f10ee01b42b
출처 메모uspto-grants-2014_11