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HRID 1060933作成日:2026年10月27日

4-(3-(4-fluorophenyl)-1H-pyrazol-4-yl]-N-[(4-methoxyphenyl)methyl]-2-pyrimidinamine → 4-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]-2-pyrimidinamine

https://huagongshe.com/reaction/1060933

反応式

関与物質

役割名称HCID仕込み量
反応物4-(3-(4-fluorophenyl)-1H-pyrazol-4-yl]-N-[(4-methoxyphenyl)methyl]-2-pyrimidinamineHCID 178490982—
溶媒Trifluoroacetic acidHCID 6422—
生成物4-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]-2-pyrimidinamineHCID 178508385—

反応手順

A solution of 4-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]-N-[(4-methoxyphenyl)methyl]-2-pyrimidinamine prepared in accordance with Example A-305 (0.35 g, 0.00093 mol) in 15 mL of trifluoroacetic acid was heated at reflux for 16 hours. Solvent was removed and the residue was partitioned between ethyl acetate and 1 N ammonia hydroxide. Organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated and purified by chromatography on silica gel (ethyl acetate) to give 0.14 g of product, 4-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]-2-pyrimidinamine, as a pale yellow solid (59% yield), mp: 273-274° C.; Anal. Calc'd for C13H10FN5 0.25 H2O: C, 60.11; H, 4.07; N, 26.96. Found: C, 60.15; H, 3.82; N, 26.38.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06525059B1
出典データセットuspto-grants-2003_02
ORD IDord-273bf030f95243c596a776892a2a5cea
出典メモuspto-grants-2003_02