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HRID 604356作成日:2026年10月25日

Sodium Acetate → Methyl 3-(methylthio)-5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylate

https://huagongshe.com/reaction/604356

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium AcetateHCID 517045—
反応物Methyl 5-bromo-2-(methylsulfanyl)pyrimidine-4-carboxylateHCID 2794729—
反応物[2-Amino-4-(methoxycarbonyl)phenyl]boronic acid--hydrogen chloride (1/1)HCID 16427083—
溶媒DimethylformamideHCID 6228—
生成物Methyl 3-(methylthio)-5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylateHCID 5750064479.6%

反応条件

温度120 °C

反応手順

In a microwave vessel, methyl 5-bromo-2-(methylthio)pyrimidine-4-carboxylate (1.0 eq, 274 mg, 1.18 mmol), 2-amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride (1.2 eq, 329 mg, 1.42 mmol), and sodium acetate (3.0 eq, 291 mg, 3.55 mmol) were mixed in anhydrous DMF (2 ml). The mixture was degassed by bubbling nitrogen gas in the solution for 10 min and the reaction heated under microwaves at 120° C. for 30 min. After cooling down the expected material crashed out of NMP. The solid was filtered, suspended in water filtered and dried. The material was triturated in AcOEt and filtered give a yellow solid. The same procedure was repeated 9 times using the same amounts of materials to provide methyl 3-(methylthio)-5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylate (283 mg, 10% yield). LCMS (ES): >95% pure, m/z 302 [M+l]+, 1H NMR (DMSO-d6, 400 MHz) δ 2.71 (s, 3H), 3.89 (s, 3H), 7.80 (dd, J=1.6, J=8.4, 1H), 7.97 (d, J=1.6, 1H), 8.59 (d, J=8.8, 1H), 9.98 (s, 1H), 12.34 (s, 1H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07910600B2
出典データセットuspto-grants-2011_03
ORD IDord-5b27198be77b46d88b08548eabb3428a
出典メモuspto-grants-2011_03