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HRID 2359734作成日:2026年10月25日

Dimethylformamide → 4'-(Cyclopropylmethyl)-N-methyl-2-(methylthio)-[4,5'-bipyrimidin]-2'-amine

https://huagongshe.com/reaction/2359734

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物(3Z)-1-Cyclopropyl-4-(dimethylamino)-3-[2-(methylsulfanyl)pyrimidin-4-yl]but-3-en-2-oneHCID 67983763—
反応物HCID 178485088HCID 178485088—
生成物4'-(Cyclopropylmethyl)-N-methyl-2-(methylthio)-[4,5'-bipyrimidin]-2'-amineHCID 6798389886%

反応手順

A solution of (3Z)-1-cyclopropyl-4-(dimethylamino)-3-[2-(methylsulfanyl)pyrimidin-4-yl]but-3-en-2-one (3) (810 mg, 2.92 mmol), N-methylguanidine (480 mg, 4.38 mmol), and K2CO3 (1211 mg, 8.76 mmol) in DMF (28 mL) was stirred at 120° C. for 2 hours, followed by stirring at rt for 18 hours. The reaction was partitioned between water and EtOAc. The organic layer was separated, and the aqueous layer was back-extracted. The organic extracts were combined, washed with brine, dried over sodium sulfate, then concentrated in vacuo. The crude product was purified by Biotage™ silica gel chromatography [100 g SNAP column, 30% EtOAc/heptane to 100% EtOAc] to afford the desired product as a white solid (720 g, 86% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 0.12 (br. s., 2H) 0.37 (d, J=7.07 Hz, 2H) 1.07 (br. s., 1H) 2.81 (d, J=6.57 Hz, 2H) 2.87 (d, J=5.05 Hz, 3H) 7.39 (d, J=5.05 Hz, 1H) 7.49 (br. s., 1H) 8.49 (br. s., 1H) 8.60 (d, J=5.05 Hz, 1H). MS (ES+): m/z=288.2/289.2/290.2 (100/20/10) [MH+]. HPLC: tR=1.28 minutes over 3 minutes. Purity: 100% [HPLC (LC/MS) at 220 nm].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08685993B2
出典データセットuspto-grants-2014_04
ORD IDord-1f2c55c167574e9597e3ddb13b91c9af
出典メモuspto-grants-2014_04