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HRID 18084作成日:2026年10月25日

tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylate → (S)-2-[(6,7-Difluoro-3-methylquinoxaline-2-ylamino)methyl]-piperidine-1-carboxylic acid tert butylester

https://huagongshe.com/reaction/18084

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylateHCID 1502020—
反応物2-Chloro-6,7-difluoro-3-methylquinoxalineHCID 10220011—
溶媒DimethylformamideHCID 6228—
生成物(S)-2-[(6,7-Difluoro-3-methylquinoxaline-2-ylamino)methyl]-piperidine-1-carboxylic acid tert butylesterHCID 86593671—

反応条件

温度90 °C

反応手順

(S)-2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (1.14 g), and 2-chloro-6,7-difluoro-3-methylquinoxaline Teng et al PCT Int. Appl (2000), WO00/42026A1 20000720 (1.14 g) were dissolved in DMF (2 ml) and heated to 90° C. for 3 days under an atmosphere of argon. After cooling, the reaction solution was partitioned between ethyl acetate and water. The organic layer was washed with water, saturated brine, dried and evaporated. The residue was chromatographed over silica gel, eluting with a gradient of 10 to 50% ethyl acetate in hexane. The title compound was obtained as a pink foam (0.524 g), MH+ 393.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741329B2
出典データセットuspto-grants-2010_06
ORD IDord-e387087c8a394279bd035d0d571cc60a
出典メモuspto-grants-2010_06