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HRID 76401作成日:2026年10月24日

4-Ethoxyaniline → N2-(4-Ethoxyphenyl)-5-methoxycarbonyl-4-trifluoromethyl-2-pyrimidineamine

https://huagongshe.com/ja/reaction/76401

反応式

関与物質

役割名称HCID仕込み量
反応物4-EthoxyanilineHCID 9076—
反応物Methyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylateHCID 3696469—
反応物N2-(2-ethoxyphenyl)-5-methoxycarbonyl-4-trifluoromethyl-2-pyrimidineamineHCID 22060734—
生成物N2-(4-Ethoxyphenyl)-5-methoxycarbonyl-4-trifluoromethyl-2-pyrimidineamineHCID 22060255—

反応手順

In like manner to the preparation of N-(2-chloro-5-ethoxycarbonyl-4-pyrimidinyl)-L-phenylalanine Ethyl Ester, 2-chloro-5-methoxycarbonyl-4-trifluoromethylpyrimidine and 4-ethoxyaniline were reacted to prepare N2-(2-ethoxyphenyl)-5-methoxycarbonyl-4-trifluoromethyl-2-pyrimidineamine. 1H NMR (CDCl3): δ 8.98 (s, 1H), 7.47 (m, 3H), 6.91 (dd, 2H, J=2.1 and 6.9 Hz), 4.05 (q, 2H, 6.9 Hz), 1.42 (t, 3H, J=6.8 Hz); 19F NMR (CDCl3): −19105; LCMS: ret. time: 33.87 min; purity: 100%; MS (m/e): 342 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835430B2
出典データセットuspto-grants-2014_09
ORD IDord-769f46a9baeb449ba95f4a3c48896660
出典メモuspto-grants-2014_09