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HRID 18082作成日:2026年10月24日

Diisopropylethylamine → 2-(Quinazolin-4-ylaminomethyl)-piperidine-1-carboxylic acid tert butyl ester

https://huagongshe.com/ja/reaction/18082

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylateHCID 1502020—
反応物4-ChloroquinoxalineHCID 86626011—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Quinazolin-4-ylaminomethyl)-piperidine-1-carboxylic acid tert butyl esterHCID 86626604—

反応手順

(S)-2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (1.0 g), 4-chloroquinoxaline (0.768 g) and diisopropylethylamine (0.816 ml) were dissolved in tetrahydrofuran (75 ml) and heated to reflux for 6 hours under an atmosphere of argon. After cooling, the reaction solution was partitioned between ethyl acetate and water. The organic layer was washed with saturated sodium hydrogen carbonate solution, saturated brine, dried and evaporated. The residue was chromatographed over silica gel, eluting with a gradient of 50 to 100% ethyl acetate in hexane. The title compound was obtained as a white foam (1.44 g).

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-43773e5d2c34440ca5b5489610e464ec
出典メモuspto-grants-2010_06