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HRID 1412002作成日:2026年10月27日

Dimethylformamide → tert-Butyl 2-(3-(2,5-Dimethyl-1H-pyrrol-1-yl)-5-(methoxy(methyl)carbamoyl)-1H-pyrazol-1-yl)ethylcarbamate

https://huagongshe.com/reaction/1412002

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium CarbonateHCID 10340—
反応物N-Boc-2-chloroethylamineHCID 3795708—
反応物3-(2,5-Dimethyl-1H-pyrrol-1-yl)-N-methoxy-N-methyl-1H-pyrazole-5-carboxamideHCID 86684046—
溶媒WaterHCID 962—
生成物tert-Butyl 2-(3-(2,5-Dimethyl-1H-pyrrol-1-yl)-5-(methoxy(methyl)carbamoyl)-1H-pyrazol-1-yl)ethylcarbamateHCID 8668452366%

反応条件

温度110 °C

反応手順

A 250-mL round-bottomed flask equipped with a magnetic stirrer was charged with 287c (10.4 g, 1.0 eq., 41.9 mmol), tert-butyl 2-chloroethylcarbamate (37.7 g, 5.0 eq., 210.0 mmol), Na2CO3 (22.3 g, 5.0 eq., 210.0 mmol), and DMF (100 mL). The reaction mixture was stirred at 110° C. overnight. After cooling to room temperature, the resulting mixture was poured into water (200 mL) and extracted with ethyl acetate (3×100 mL). The combined organic layer was concentrated under reduced pressure. The resulting residue was purified by silica-gel column chromatography eluting with ethyl acetate to afford 287d (10.8 g, 66%) as yellow oil. MS-ESI: [M+H]+ 392.0

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921353B2
出典データセットuspto-grants-2014_12
ORD IDord-a97d1c1702154275b4ad7714984e7d7b
出典メモuspto-grants-2014_12