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HRID 2287721作成日:2026年10月25日

2-(Trifluoromethyl)benzylamine → Pyrido[4,3-d]pyrimidine-4,7-diamine,n4-[[2-(trifluoromethyl)phenyl]methyl]-

https://huagongshe.com/reaction/2287721

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Trifluoromethyl)benzylamineHCID 76447—
反応物7-Amino-4-methylthiopyrido[4,3-d]pyrimidineHCID 10442562—
生成物Pyrido[4,3-d]pyrimidine-4,7-diamine,n4-[[2-(trifluoromethyl)phenyl]methyl]-HCID 532808459%

反応条件

温度150 °C

反応手順

A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (225 mg, 1.17 mmol) and 2-(trifluoromethyl)benzylamine (0.90 mL, 6.42 mmol) is stirred under N2 at 150° C. for 1 h. The resulting product is chromatographed on silica gel (5% EtOH/EtOAc) to give 7-amino-4-(2-trifluoromethylbenzyl) aminopyrido[4,3-d]pyrimidine (0.22 g, 59%) as a white solid. 1H NMR (DMSO) δ 9.16 (1H, s), 8.88 (1H, t, J=5.7 Hz), 8.23 (1H, s), 7.75 (1H, d, J=7.7 Hz), 7.62 (1H, t, J=7.5 Hz), 7.50 (1H, d, J=7.4 Hz), 7.47 (1H, t, J=7.6 Hz), 6.51 (2H, brs), 6.39 (1H, s), 4.92 (2H, d, J=5.5 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06084095
出典データセットuspto-grants-2000_07
ORD IDord-e891d0607f824cd5865d7b2fec4573b6
出典メモuspto-grants-2000_07