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HRID 603864作成日:2026年10月24日

3-Amino-N-methylbenzamide → 5-fluoro-N4-[(1H)indol-6-yl]-N2-[3-[(N-methylamino)carbonyl]phenyl]-2,4-pyrimidinediamine

https://huagongshe.com/ja/reaction/603864

反応式

関与物質

役割名称HCID仕込み量
反応物3-Amino-N-methylbenzamideHCID 676526—
反応物2-chloro-5-fluoro-N4-[(1H)indol-6-yl]-4-pyrimidineamineHCID 22060459—
生成物5-fluoro-N4-[(1H)indol-6-yl]-N2-[3-[(N-methylamino)carbonyl]phenyl]-2,4-pyrimidinediamineHCID 22060488—

反応手順

In like manner to the preparation of 5-fluoro-N4-(3-hydroxyphenyl)-N2-[4-(3-phenyl-1,2,4-oxadiazol-5-yl)methyleneoxyphenyl]-2,4-pyrimidinediamine, 2-chloro-5-fluoro-N4-[(1H)indol-6-yl]-4-pyrimidineamine and 3-[(N-methylamino)carbonyl]aniline were reacted to provide 5-fluoro-N4-[(1H)indol-6-yl]-N2-[3-[(N-methylamino)carbonyl]phenyl]-2,4-pyrimidinediamine. 1H NMR (CD3OD): δ 7.99 (t, 1H, J=1.8 Hz), 7.89 (d, 1H, J=3.6 Hz), 7.78-7.76 (m, 1H), 7.70 (ddd, 1H, J=1.2, 2.4, and 8.4 Hz), 7.50 (d, 1H, J=9.0 Hz), 7.31 (td, 1H, J=1.2 and 7.5 Hz), 7.23-7.17 (m, 3H), 6.43 (dd, 1H, J=1.2 and 3.6 Hz), 2.73 (s, 3H); 19F NMR (282 MHz, CD3OD): −47513; LCMS: purity: 99%; MS (m/e): 377 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906644B2
出典データセットuspto-grants-2011_03
ORD IDord-3c76b6d9f66245e4ac16f99a14276008
出典メモuspto-grants-2011_03