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HRID 50815作成日:2026年10月24日

3-(Trifluoromethyl)benzylamine → Pyrido[4,3-d]pyrimidine-4,7-diamine,n4-[[3-(trifluoromethyl)phenyl]methyl]-

https://huagongshe.com/ja/reaction/50815

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethyl)benzylamineHCID 75962—
反応物7-Amino-4-methylthiopyrido[4,3-d]pyrimidineHCID 10442562—
生成物Pyrido[4,3-d]pyrimidine-4,7-diamine,n4-[[3-(trifluoromethyl)phenyl]methyl]-HCID 532808564.2%

反応条件

温度140 °C

反応手順

A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (225 mg, 1.17 mmole) and 3-(trifluoromethyl)benzylamine (0.63 mL, 4.40 mmole) is stirred under N2 at 140° C. for 1 h. The resulting product is chromatographed on silica gel (3-5t EtOH/EtOAc) to give 7-amino-4-[(3-trifluoromethylphenyl)methylamino]pyrido[4,3-d]pyrimidin (0.24 g, 63%) as a light brown solid. 1H NMR (DMSO) δ 9.10 (1H, s), 8.92 (1H, t, J=5.7 Hz), 8.26 (1H, s), 7.71 (1H, s), 7.66 (1H, d, J=7.4 Hz), 7.62 (1H, d, J=7.8 Hz), 7.57 (1H, t, J=7.6 Hz), 6.49 (2H, brs), 6.38 (1H, s), 4.82 (2H, d, J=5.8 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713484B2
出典データセットuspto-grants-2004_03
ORD IDord-7460375d32394aeb8f646e4306e924f4
出典メモuspto-grants-2004_03