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HRID 17330作成日:2026年10月25日

Triethylamine → 6-bromo-2-cyclopropyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/reaction/17330

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物(3S)-(-)-3-(Dimethylamino)pyrrolidineHCID 7019156—
反応物6-Bromo-2-cyclopropyl-7-fluoro-5-methylbenzoxazole-4-carbonitrileHCID 51041427—
溶媒Dimethyl SulfoxideHCID 679—
生成物6-bromo-2-cyclopropyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-1,3-benzoxazole-4-carbonitrileHCID 6858595426.4%

反応条件

温度90 °C

反応手順

(3S)-3-(Dimethylamino)pyrrolidine (157 μl, 1.24 mmol) and triethylamine (348 μl, 2.50 mmol), were added to a dimethyl sulfoxide (5 ml) solution of 6-bromo-2-cyclopropyl-7-fluoro-5-methyl-1,3-benzoxazole-4-carbonitrile (I-77) (304 mg, 1.03 mmol). The system was purged with nitrogen and then sealed up and heated at 90° C. for 2 hours. After cooling, the solvent was evaporated away under reduced pressure, then the resulting residue was dissolved in chloroform, washed with water and saturated brine. The organic layer was dried over anhydrous sodium sulfate, then the solvent was evaporated away under reduced pressure, the resulting residue was washed with a mixed solvent of isopropyl ether and ethanol. The crystal was collected by filtration to obtain the entitled compound (106 mg, 26%) as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737166B2
出典データセットuspto-grants-2010_06
ORD IDord-5089e38f65e34a179fddb8f70be12570
出典メモuspto-grants-2010_06