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HRID 2362810作成日:2026年10月27日

1,3-Dichloroacetone → 2-Amino-4-{4-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}-6-[({2-[(4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]pyridine-3,5-dicarbonitrile

https://huagongshe.com/reaction/2362810

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-DichloroacetoneHCID 10793—
反応物Sodium BicarbonateHCID 516892—
反応物4-FluorophenylthioureaHCID 693061—
反応物HCID 178431437HCID 178431437—
溶媒EthanolHCID 702—
生成物2-Amino-4-{4-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}-6-[({2-[(4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]pyridine-3,5-dicarbonitrileHCID 86624334—

反応手順

102 mg (0.6 mmol) of 4-fluorophenylthiourea and 73.6 mg (0.58 mmol) of 1,3-dichloroacetone are dissolved in 2.5 ml of ethanol, and the mixture is stirred under reflux for 60 min. The mixture is allowed to cool and concentrated using a rotary evaporator. The residue is taken up in 1.5 ml of DMF, 153 mg (0.4 mmol) of the compound from Example 3A and 101 mg (1.2 mmol) of sodium bicarbonate are added and the reaction solution is stirred at RT for a further 16 h. The reaction mixture is purified directly by preparative HPLC chromatography (column: YMC GEL ODS-AQ S-5/15 μm; mobile phase gradient: acetonitrile/water 10:90→95:5).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08691850B2
出典データセットuspto-grants-2014_04
ORD IDord-4e52978ae3a14672b5123e0fbb6a7afb
出典メモuspto-grants-2014_04