戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 71433作成日:2026年10月24日

1,4-Benzodioxan-6-ylamine → N2-(3,4-ethylenedioxyphenyl)-5-fluoro-N2-(2-hydro xy-2-phenylethyl)-2,4-pyrimidinediamine

https://huagongshe.com/ja/reaction/71433

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Benzodioxan-6-ylamineHCID 89148—
反応物N4-(3,4-ethylenedioxyphenyl)-5-fluoro-N2-(3-hydroxyphenyl)-2,4-primidinediamineHCID 22060334—
反応物2-chloro-5-fluoro-N4-(2-hydroxy-2-phenylethyl)-4-pyrimidineamineHCID 22060827—
生成物N2-(3,4-ethylenedioxyphenyl)-5-fluoro-N2-(2-hydro xy-2-phenylethyl)-2,4-pyrimidinediamineHCID 22060669—

反応手順

In a manner similar to the preparation of N4-(3,4-ethylenedioxyphenyl)-5-fluoro-N2-(3-hydroxyphenyl)-2,4-pyrimidinediamine, 2-chloro-5-fluoro-N4-(2-hydroxy-2-phenylethyl)-4-pyrimidineamine and 3,4-ethylenedioxyaniline were reacted to yield N2-(3,4-ethylenedioxyphenyl)-5-fluoro-N2-(2-hydroxy-2-phenylethyl)-2,4-pyrimidinediamine. 1H NMR (CDCl3): δ 7.79 (s, 1H), 7.48 (m, 5H), 6.89-6.71 (m, 3H), 5.41-5.38, 4.97 (dd, 1H, J=3.6 and 7.5 Hz), 4.28-4.22 (m, 4H), 3.88 (ddd, 1H, J=4.2, 7.2, and 14.1), 3.64-3.55 (m, 1H); 19F NMR (CDCl3): −47910; LCMS: ret. time: 20.47 min.; purity: 88%; MS (m/e): 383 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822685B2
出典データセットuspto-grants-2014_09
ORD IDord-ff845071e59c48b1a0ca45a20b43c0cd
出典メモuspto-grants-2014_09